Efficacy and safety of acupuncture at Different depths of Qugu Acupoint in the treatment of benign prostatic hyperplasia: a randomized controlled trial

Registration number:

ITMCTR2200005751

Date of Last Refreshed on:

2022-01-01

Date of Registration:

2022-01-01

Registration Status:

Prospective registration

Public title:

Efficacy and safety of acupuncture at Different depths of Qugu Acupoint in the treatment of benign prostatic hyperplasia: a randomized controlled trial

English Acronym:

Scientific title:

Efficacy and safety of acupuncture at Different depths of Qugu Acupoint in the treatment of benign prostatic hyperplasia: a randomized controlled trial

Scientific title acronym:

Study subject ID:

The registration number of the Partner Registry or other register:

ChiCTR2200055104 ; ChiMCTR2200005751

Applicant:

Guo Wenhao

Study leader:

Lu Yonghui

Applicant telephone:

13668641997

Study leader's telephone:

13521776025

Applicant Fax:

Study leader's fax:

Applicant E-mail:

aubrey1122@163.com

Study leader's E-mail:

yhlu2008@sina.com

Study leader's website(voluntary supply):

Study leader's website
(voluntary supply):

Applicant address:

No.1 Xiyuan Playground, Haidian District, Beijing

Study leader's address:

No.1 Xiyuan Playground, Haidian District, Beijing

Applicant postcode:

Study leader's postcode:

Applicant's institution:

Xiyuan Hospital of China Academy of Chinese Medical Sciences

Approved by ethic committee:

Approved No. of ethic committee:

中国中医科学院西苑医院医学伦理委员会2021XLA101-2

Approved file of Ethical Committee:

View

Name of the ethic committee:

Medical Ethics Committee, Xiyuan Hospital, China Academy of Chinese Medical Sciences

Date of approved by ethic committee:

2021/11/25 0:00:00

Contact Name of the ethic committee:

Zi Mingjie

Contact Address of the ethic committee:

No.1 Xiyuan Playground, Haidian District, Beijing

Contact phone of the ethic committee:

Contact email of the ethic committee:

Primary sponsor:

Xiyuan Hospital of China Academy of Chinese Medical Sciences

Primary sponsor's address:

No.1 Xiyuan Playground, Haidian District, Beijing

Secondary sponsor:

Country:

China

Province:

Beijing

City:

Institution
hospital:

Xiyuan Hospital of China Academy of Chinese Medical Sciences

Address:

No.1 Xiyuan Playground, Haidian District, Beijing

Source(s) of funding:

China Academy of Chinese Medical Sciences

Target disease:

Benign Prostatic Hyperplasia

Target disease code:

Study type:

Interventional study

Study design:

randomized controlled trial(parallel group design)

Study phase:

Phase I clinical trial

Objectives of Study:

To provide evidence-based medical evidence of the efficacy and safety of "acupuncture at different depths of qu Bone point" in the treatment of benign prostatic hyperplasia

Description for medicine or protocol of treatment in detail:

Inclusion criteria

(1)It meets the diagnostic criteria of BPH and has been clearly diagnosed by a specialist; (2)The age ranges from 50 to 80; (3)Voluntary subjects who sign informed consent voluntarily.

Exclusion criteria:

(1) Unable to communicate unobstructed; (2) Associated with urethritis, acute prostatitis, urinary calculi and other diseases; (3) Complicated with neurogenic bladder, bladder neck fibrosis, urethral stricture and other diseases; (4) Patients with neurological diseases or diabetes that affect urination function; (5) Hyperplasia of prostate complicated with malignant wasting diseases such as prostate cancer and tuberculosis; (6) Patients with serious diseases such as liver and kidney insufficiency and other heart and lung diseases and blood diseases; (7) Patients taking anticoagulants for a long time and patients with severe anemia; (8) Patients with upper urinary tract obstruction and hydronephrosis and impaired renal function found by B-ultrasound; (9) Have been using drugs that may affect bladder function or are receiving BPH drugs; (10) B ultrasound or CT found excessive prostatic hyperplasia, protruding too much bladder, affecting acupuncture operators; (11) B ultrasound or CT found that residual urine in the bladder was more than 100ml or too much, which affected the acupuncture operator.

Study execute time:

From 2022-01-01

To      2024-10-31

Recruiting time:

From 2022-01-01

To      2023-12-31

Interventions:

40

Group:

The treatment group2

Sample size:

Intervention:

Acupuncture is inserted into the abdominal wall

Intervention code:

40

Group:

Control group

Sample size:

Intervention:

Acupuncture is inserted into the superficial fascia

Intervention code:

40

Group:

The treatment group1

Sample size:

Intervention:

Acupuncture is inserted into the prostate capsule

Intervention code:

Total sample size : 120

Countries of recruitment
and research settings:

Country:

China

Province:

Beijing

City:

Institution/hospital:

Xiyuan Hospital of China Academy of Chinese Medical Sciences

Level of the institution:

Grade Ⅲ, Class A

Outcomes:

Outcome:

Quality of life,QoL

Type:

Secondary indicator

Measure time point of outcome:

Measure method:

Outcome:

International Prostate Symptom Score,IPSS

Type:

Primary indicator

Measure time point of outcome:

Measure method:

Collecting sample(s)
from participants:

Sample Name:

Blood

Tissue:

Fate of sample 

Destruction after use

Note:

Sample Name:

Urine

Tissue:

Fate of sample 

Destruction after use

Note:

Not yet recruiting

50
Min age years
80
Max age years

Recruiting status:

Participant age:

Gender:

Male

Randomization Procedure (please state who generates the random number sequence and by what method):

Using the method of block randomization, with the help of SPSS18.0 statistical analysis software, the random number grouping table is generated, which is kept by statisticians. Random number table The concealment of the random assignment scheme used sequentially coded, sealed, opaque envelopes to randomly assign subjec

Blinding:

IPD sharing:

Yes

The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url):

No

Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture:

Case Report Form The version number:VERSION 1.0_20211019 Random encoding : |__|__|__|__| Subject's initials : |__|__|__|__| Name of Doctor (in Block letters): ___ Study time: October 2021 -- October 2024 Instructions for filling in the case report form (Please read the following instructions carefully before completing this form.) 1、This case report form must be filled in by a full-time evaluator and completed by the same person as far as possible;The doctor's signature on the front and end pages should be filled in by the investigator in charge of the case. 2、A large number of data in this CRF are obtained from the statistics, calculation and summary of the original data (subjects' urination diary card, etc.). Please be sure to check carefully and make accurate statistics and calculation to avoid manual statistical errors! 3、The subject enrollment number on the upper right corner of the cover is compiled by the researcher to facilitate monitoring and CRF management. 4、Please complete this form with pen or marker pen, not pencil or ballpoint pen. 5、The qualified candidates shall formally fill in the case report form, and the last data shall be carried forward as the last data for those who have stopped treatment, and the time and reason of withdrawal shall be truthfully recorded. 6、If there is a "□" in the table, please put an "×" in the correct "□". 7、Please fill in the number in the open box, one number in each box, if the number is not enough, please filling 0 in the front or back box. All inspection items must be filled in. Please fill in "ND" if there is no inspection/omission for some reason. Data unknown/not known, please fill in "UK"; If this option is not applicable, enter NA. 8、Method of filling in the name of the subject: The abbreviation of the name of the subject should be filled in four squares, and the first two letters of the name of the subject should be filled in the first two letters of each pinyin; Fill in the first letter and the second letter of the third word pinyin for the three-character name; Fill in the first letter of the four-character name in their pinyin; Fill in the first letter of the first four characters in pinyin. The investigator must complete a subject identity registration form to facilitate identification of subjects during and after the trial. 9、Be sure to fill in accurately and clearly, do not erase or alter at will, correct the mistakes with a horizontal line in the center, and sign the name of the modifier (physician's initials, capital letters) and the modification time, and explain the reason if necessary. Do not mask the original data you fill in, and do not allow erasers, correction fluids, or scratching out the original content. Example: fill in the wrong 2011/07/13/[year, month, day], correction model 2011/07/1314 SJF 2011/07/14 . 10、The international IS08601 date format is yyyymmdd. For example: October 15, 2010 written: 20101015. Use medical terminology when describing history and adverse events. Use the full name of the diagnosis and drug. Do not use abbreviations or abbreviations unless they are listed in the study protocol. 11、Please strictly implement the clinical trial plan, and the projects to be completed at each visit site should be carried out according to the clinical study flow chart, and pay attention to the time window. 12、The combined medication record form and adverse reaction/event record form should be truthfully filled in during the clinical study. If a serious adverse event occurs, a serious adverse event record form must be filled in regardless of whether the event is related to the study treatment or not, along with the usual treatment. Clinical study flowchart Phase Baseline (Weeks 1-4) Treatment time( Weeks 5-8) Follow-up 5 weeks 6 weeks 7 weeks 8 weeks 16 weeks 32 weeks Treatment 0 3 times 3 times 2 times 2 times International Prostatic Symptom Scale (IPSS) √ √ √ √ √ Quality of Life evaluation (QoL) √ √ √ √ √ Prostate volume(cm3) √ √ Post-void residual PVR(ml) √ √ Maximum flow rate Qmax(ml/s) √ √ Digital Rectal Examination(DRE) √ √ Informed consent √ Evaluation method for the blind √ √ Acupuncture safety √ √ Acupuncture resistance √ √ Emergency medicine Adverse events Note: 1. "√" in this table represents the projects that must be completed by this time node. 2. In case of intermediate shedding, the most recent specialized evaluation data of the subject should be traced back as far as possible, and the phase table should be filled in in time, and the reduction loss rate should be tabled to reduce the data loss rate. 3. After observation and observation, 1 internal observation shall be audited and signed by the person in charge within a week. 4. The supervisor of the project undertaking unit shall regularly inspect and review all RCRF entry and approval forms. First visit (1-4 weeks) Date of visit:20 |__|__|year|__|__|month|__|__|day Note: This date should be the date of randomization after the baseline screening of the subject (the date of enrollment). Other visit times should be based on this date. Date of signing informed consent: 20 |__|__|year|__|__|month|__|__|day Inclusion Criteria (If "no" is selected for any item, it will not be included in this study) Yes No 1.Meet the diagnostic criteria of BPH. ¨1 ¨0 2.Age range: 50 to 80. ¨1 ¨0 3.Those who voluntarily sign informed consent are required to participate in this study. ¨1 ¨0 Exclusion criteria (" Yes "means no inclusion in this study) Yes No 1.Unable to communicate unobstructed. ¨1 ¨0 2.Associated with urethritis, acute prostatitis, urinary calculi and other diseases. ¨1 ¨0 3.Complicated with neurogenic bladder, bladder neck fibrosis, urethral stricture and other diseases. ¨1 ¨0 4.Patients with neurological diseases or diabetes that affect urination function. ¨1 ¨0 5.Hyperplasia of prostate complicated with malignant wasting diseases such as prostate cancer and tuberculosis. ¨1 ¨0 6.Patients with serious diseases such as liver and kidney insufficiency and other heart and lung diseases and blood diseases. ¨1 ¨0 7.Patients with upper urinary tract obstruction and hydronephrosis and impaired renal function found by B-ultrasound. ¨1 ¨0 8.Have been using drugs that may affect bladder function or are receiving BPH drugs. ¨1 ¨0 9.B ultrasound or CT found excessive prostatic hyperplasia affecting acupuncture operators. ¨1 ¨0 10.B ultrasound or CT found that residual urine in the bladder was too much, which affected the acupuncture operator. ¨1 ¨0 TCM syndromes Kidney qi depletion Center qi fall Qi stagnation and blood stasis Damp-heat brewing and binding Kidney vacuity and blood stasis Kidney vacuity and damp-heat Damp-heat and blood stasis Dual vacuity of the spleen and kidney Demographic data Gender Men Date of birth |__|__|__|__|year |__|__|month|__|__|day CT serial number National ¨1 The Han nationality ¨2 The Zhuang nationality ¨3 The Zhuang nationality ¨4 The Hui nationality ¨5 The Miao nationality ¨6 The Uygur nationality ¨7 other____ Marital status ¨1 Yes ¨2 No Degree ¨1 Postgraduate and above ¨2 Undergraduate ¨3 College Specialist ¨4 High school/Secondary school/Technical school ¨5 Junior high school ¨6 Primary school ¨7 Illiteracy Occupation ¨1 Worker ¨2 Farmer ¨3 Teacher ¨4 Solider ¨5 Student ¨6 Cadre ¨7 Employee ¨8 Retired ¨9 Freelance ¨10 Other____ Height |__|__|__|.|__|cm Weight |__|__|__|.|__|kg Body mass index(BMI) |__|__|.|__| Distance between the anterior superior iliac spine on both sides |__|__|__|.|__|cm Waist at navel level |__|__|__|.|__|cm Symphysis pubis is horizontally positioned around the buttocks |__|__|__|.|__|cm Formula acupuncture depth |__|__|__|.|__|mm Formula acupuncture Angle |__|__|.|__|Angle Acupuncture depth under CT |__|__|__|.|__|mm Acupuncture Angle under CT |__|__|.|__|Angle Contact Number 1: Contact Number 2: Address: Benign Prostatic Hyperplasia(BPH)Medical history Course of the disease |__|__|year|__|__|month The degree of BPH ¨1 Mild ¨2 Moderate ¨3 Severe Concomitant disease ¨1No ¨2 Yes, please continue to fill in the form below. Name of co-morbidities The start time The end of time |__|__|__|__|year|__|__|month |__|__|__|__|year|__|__|month Treatment of BPH Whether or not to receive treatment for BPH: ¨1No ¨2 Yes, please continue to fill in the form below. Treatment ¨1Traditional Chinese medicine treatment ¨2Western medicine treatment ¨3The surgical treatment ¨4Other Last treatment |__|__|__|__|year|__|__|month|__|__|day-|__|__|__|__|year|__|__|month|__|__|day Drugs in use BPH therapy:___________; Other therapeutic drugs :_____________. Ultrasonic prostate volume and postvoid residual urine volume |__|__|__|__|year|__|__|month|__|__|day Volume|__|__|__|.|__|ml, post-void residual |__|__|__|ml |__|__|__|__|year|__|__|month|__|__|day Volume |__|__|__|.|__|ml, post-void residual |__|__|__|ml Determination of maximum flow rate |__|__|__|__|year|__|__|month|__|__|day,_________ml/s |__|__|__|__|year|__|__|month|__|__|day, _________ml/s Efficacy evaluation index 1 2 3 4 5 International Prostate Symptom Scale(IPSS) Symptom sign and examination score Quality of Life score (QoL) Acupuncture tolerance score Questionnaire at baseline during the first visit(Week1-4) Date of visit: 20 |__|__|year|__|__|month|__|__|day Table 1 International Prostate Symptom Scale (IPSS) Have you had any of the following symptoms in the last 1 month? No In the five times Symptom scores Less than 1/5 Less than 1/2 About 1/2 More than half Almost always 1. Do you often feel like urination is not enough? 0 1 2 3 4 5 2.Are two urination intervals often less than 2 hours? 0 1 2 3 4 5 3.Do you often have intermittent urination? 0 1 2 3 4 5 4.Whether there is a phenomenon of urination cannot wait? 0 1 2 3 4 5 5.Is there any narrowing of urinary line? 0 1 2 3 4 5 6.Do you need to exert force to start urination? 0 1 2 3 4 5 7. How many times do you need to get up and urinate from falling asleep to getting up early? No Once Twice 3 times 4 times 5 times 0 1 2 3 4 5 IPSS Total score= Table 2 Quality of Life(QoL)Scale Symptoms Happy Satisfied Generally satisfied So-so Not satisfied distress Very bad What do you think if you have urination symptoms for the rest of your life? 0 1 2 3 4 5 6 Quality of Life (QoL) Table 4 Symptom signs and auxiliary examination grading scoring standard 0 1 2 3 Score IPSS 0 1-7 8-19 20-35 DRE Normal Ⅰ° Ⅱ° Ⅲ° QoL 0-1 2 3-4 5-6 Prostate volume(cm3) <18 18 ~ 25 26 ~ 45 > 46 PVR(ml) ≤10 11 ~ 60 61 ~ 100 > 100 Qmax(ml/s) > 15 10.1~15 5 ~ 10 < 5 Nocturnal urine frequency (times) 0 ~ 1 2 3 ~ 4 ≥5 Urine line status Normal Urinary fine such as line Urine into line Little drops do not make a thread Small abdominal distension full No Occasionally Sometimes Often Urine waiting No Occasionally Sometimes Often Urine urgency No Can endure Bear with me for a while Can't stand Total score Questionnaire 2 weeks after the second visit(Week5-6) Date of visit: 20 |__|__|year|__|__|year|__|__|day Is the visit on schedule? ¨1Yes ¨0No The reason for the delay: Table 1 International Prostate Symptom Scale (IPSS) Have you had any of the following symptoms in the last 1 month? No In the five times Symptom scores Less than 1/5 Less than 1/2 About 1/2 More than half Almost always 1. Do you often feel like urination is not enough? 0 1 2 3 4 5 2.Are two urination intervals often less than 2 hours? 0 1 2 3 4 5 3.Do you often have intermittent urination? 0 1 2 3 4 5 4.Whether there is a phenomenon of urination cannot wait? 0 1 2 3 4 5 5.Is there any narrowing of urinary line? 0 1 2 3 4 5 6.Do you need to exert force to start urination? 0 1 2 3 4 5 7. How many times do you need to get up and urinate from falling asleep to getting up early? No Once Twice 3 times 4 times 5 times 0 1 2 3 4 5 IPSS Total score= Table 2 Quality of Life(QoL)Scale Symptoms Happy Satisfied Generally satisfied So-so Not satisfied distress Very bad What do you think if you have urination symptoms for the rest of your life? 0 1 2 3 4 5 6 Quality of Life (QoL) Table 3 Acupuncture safety evaluation and acupuncture tolerance evaluation Safety evaluation of acupuncture(Record each treatment at any time)¨1No ¨2 Yes, please continue to fill out this form Symptom code/name occurrences Other discomfort after acupuncture Duration |__|__| |__|__| |__|__| 01= Broken needle, 02= Needle stagnation, 03= needle phobia, 04= Local hematoma, 05= Local infection, 06= Local abscess, 07= Pain. Other discomfort after acupuncture: 08= Fatigue, 09= Heart palpitations, 10= Dizzy, 11= Headache, 12= Insomnia, 13=Other: Evaluation method for the blind (Evaluation after the first treatment) Acupuncture treatment ¨1Yes ¨0No Evaluation of acupuncture tolerance(Evaluation after the first treatment) Evaluation of acupuncture discomfort No discomfort 0--1--2--3--4--5--6--7--8--9--10 Very uncomfortable ¨¨ Evaluation of acupuncture tolerance ¨0 very difficult to accept ¨1 Take it a little harder ¨2 Can accept ¨3 Easy to accept ¨4 Very receptive Third visit questionnaire after 4 weeks of treatment(5-8周) Date of visit:20 |__|__|year|__|__|month|__|__|day Is the visit on schedule? ¨1Yes ¨0No?The reason for the delay: Table 1 International Prostate Symptom Scale (IPSS) Have you had any of the following symptoms in the last 1 month? No In the five times Symptom scores Less than 1/5 Less than 1/2 About 1/2 More than half Almost always 1. Do you often feel like urination is not enough? 0 1 2 3 4 5 2.Are two urination intervals often less than 2 hours? 0 1 2 3 4 5 3.Do you often have intermittent urination? 0 1 2 3 4 5 4.Whether there is a phenomenon of urination cannot wait? 0 1 2 3 4 5 5.Is there any narrowing of urinary line? 0 1 2 3 4 5 6.Do you need to exert force to start urination? 0 1 2 3 4 5 7. How many times do you need to get up and urinate from falling asleep to getting up early? No Once Twice 3 times 4 times 5 times 0 1 2 3 4 5 IPSS Total score= Table 2 Quality of Life(QoL)Scale Symptoms Happy Satisfied Generally satisfied So-so Not satisfied distress Very bad What do you think if you have urination symptoms for the rest of your life? 0 1 2 3 4 5 6 Quality of Life (QoL) Table 3 Acupuncture safety evaluation and acupuncture tolerance evaluation Safety evaluation of acupuncture(Record each treatment at any time)¨1No ¨2 Yes, please continue to fill out this form Symptom code/name occurrences Other discomfort after acupuncture Duration |__|__| |__|__| |__|__| 01= Broken needle, 02= Needle stagnation, 03= needle phobia, 04= Local hematoma, 05= Local infection, 06= Local abscess, 07= Pain. Other discomfort after acupuncture: 08= Fatigue, 09= Heart palpitations, 10= Dizzy, 11= Headache, 12= Insomnia, 13=Other: Evaluation method for the blind (Evaluation after the first treatment) Acupuncture treatment ¨1Yes ¨0No Evaluation of acupuncture tolerance(Evaluation after the first treatment) Evaluation of acupuncture discomfort No discomfort 0--1--2--3--4--5--6--7--8--9--10 Very uncomfortable ¨¨ Evaluation of acupuncture tolerance ¨0 very difficult to accept ¨1 Take it a little harder ¨2 Can accept ¨3 Easy to accept ¨4 Very receptive Table 4 Symptom signs and auxiliary examination grading scoring standard 0 1 2 3 Score IPSS 0 1-7 8-19 20-35 DRE Normal Ⅰ° Ⅱ° Ⅲ° QoL 0-1 2 3-4 5-6 Prostate volume(cm3) <18 18 ~ 25 26 ~ 45 > 46 PVR(ml) ≤10 11 ~ 60 61 ~ 100 > 100 Qmax(ml/s) > 15 10.1~15 5 ~ 10 < 5 Nocturnal urine frequency (times) 0 ~ 1 2 3 ~ 4 ≥5 Urine line status Normal Urinary fine such as line Urine into line Little drops do not make a thread Small abdominal distension full No Occasionally Sometimes Often Urine waiting No Occasionally Sometimes Often Urine urgency No Can endure Bear with me for a while Can't stand Total score Follow-up questionnaire 2 months after the end of the fourth visit(Week9-16) Date of visit: 20 |__|__|year|__|__|month|__|__|day Is the visit on schedule? ¨1Yes ¨0No?The reason for the delay: Table 1 International Prostate Symptom Scale (IPSS) Have you had any of the following symptoms in the last 1 month? No In the five times Symptom scores Less than 1/5 Less than 1/2 About 1/2 More than half Almost always 1. Do you often feel like urination is not enough? 0 1 2 3 4 5 2.Are two urination intervals often less than 2 hours? 0 1 2 3 4 5 3.Do you often have intermittent urination? 0 1 2 3 4 5 4.Whether there is a phenomenon of urination cannot wait? 0 1 2 3 4 5 5.Is there any narrowing of urinary line? 0 1 2 3 4 5 6.Do you need to exert force to start urination? 0 1 2 3 4 5 7. How many times do you need to get up and urinate from falling asleep to getting up early? No Once Twice 3 times 4 times 5 times 0 1 2 3 4 5 IPSS Total score= Table 2 Quality of Life(QoL)Scale Symptoms Happy Satisfied Generally satisfied So-so Not satisfied distress Very bad What do you think if you have urination symptoms for the rest of your life? 0 1 2 3 4 5 6 Quality of Life (QoL) Follow-up questionnaire 6 months after the end of the fifth visit(Week 17-32) Date for visit: 20 |__|__|year|__|__|month|__|__|day Is the visit on schedule? ¨1Yes ¨0No?Reason for delay: Table 1 International Prostate Symptom Scale (IPSS) Have you had any of the following symptoms in the last 1 month? No In the five times Symptom scores Less than 1/5 Less than 1/2 About 1/2 More than half Almost always 1. Do you often feel like urination is not enough? 0 1 2 3 4 5 2.Are two urination intervals often less than 2 hours? 0 1 2 3 4 5 3.Do you often have intermittent urination? 0 1 2 3 4 5 4.Whether there is a phenomenon of urination cannot wait? 0 1 2 3 4 5 5.Is there any narrowing of urinary line? 0 1 2 3 4 5 6.Do you need to exert force to start urination? 0 1 2 3 4 5 7. How many times do you need to get up and urinate from falling asleep to getting up early? No Once Twice 3 times 4 times 5 times 0 1 2 3 4 5 IPSS Total score= Table 2 Quality of Life(QoL)Scale Symptoms Happy Satisfied Generally satisfied So-so Not satisfied distress Very bad What do you think if you have urination symptoms for the rest of your life? 0 1 2 3 4 5 6 Quality of Life (QoL) Drug combination: Were any western drugs other than BHP used during the study period? ¨0No,□1Yes,fill in the table below: Number Drug name Indications Whether medication is used for adverse events Dosage form A single dose Unit dose Dosing frequency Delivery way Start date Does the end of the study last? Yes No→End date 1 □1 2 □1 3 □1 4 □1 5 □1 6 □1 7 □1 8 □1 9 □1 Dosage form code CA=Capsule TB=Tablets GTTS=Drops AMP=Ampoule OT=Other Unit code of dosage form ug=Microgram mg=Milligram ml=Milliliter g= Gram OT=Other Dosing frequency code QD=Once daily BID=Twice daily TID=3 times daily QID=4 times daily QOD=Every other day QN=Once a night Q8H=Every 8 hours Q12H=Every 12 hours PRN=When necessary OT=Other Route of administration code PO=Take orally TOP=Topical SC=Subcutaneous IV=Intravenous IM=Intramuscular PR=Rectal administration NG=Nasal feeding IT=Intrathecal IA=Intra-articular SL=Sublingual INH=Inhalation IO=Intraocular TD=Percutaneous OT=Other Adverse events: Were there any adverse events throughout the study period? (Except for the discomfort listed in the safety evaluation) Have you experienced any discomfort since your last treatment? ¨0No, ¨1Yes, fill in the following form: Number Description of adverse events Does the end of the study last? severity Correlation with acupuncture treatment Measures taken for acupuncture treatment Take other measures outcome Whether or not SAE? Yes No→End date No Yes→End date 1 □0 2 □0 3 □0 4 □0 5 □0 6 □0 7 □0 8 □0 9 □0 Association of adverse events with acupuncture treatment 1=Definitely relevant 2=Probably related 3=May be relevant 4=May not be relevant 5=Definitely irrelevant Measures taken for acupuncture treatment 1=not applicable 2=No change 3=Reduce frequency /Reduces irritation 4=Pause the needle stabbing treatment 5=Stop acupuncture permanently Take other measures 1=No 2=For hospitalization or extended hospitalization, fill out SAE form 3=For combined medication, fill in the area of combined medication 4=Please describe others. The outcome of AE 1=Recovery, no sequelae 2=Recovery, with sequelae 3=Ease 4=Continuous/no change 5=Aggravation/deterioration 6=Death 7=The unknown The specific type of SAE 1=Cause of death 2=Life-threatening 3=Resulting in or prolonged hospitalization 4=Cause permanent or significant disability/loss of function 5=Cause congenital malformations 6=Other important medical events Summary of research completion Date of first treatment: 20 |__|__|year|__|__|month|__|__|day Date of last treatment: 20 |__|__|year|__|__|month|__|__|day Whether the subjects completed the 4-week study according to the study protocol ¨1Yes ¨0No, end date:20 |__|__|year|__|__|month|__|__|day, and fill in the following reasons for the suspension of the test. The main reasons for the suspension of the trial are: (choose one of the most important reasons) ¨1Breach of protocol (any breach of protocol will be assessed by the investigator to determine whether it is serious enough to withdraw from the study), please describe in detail_____________ ¨2Adverse events, number|__|__|(Adverse event form has been filled out.) ¨3Although there were no adverse events, discontinuation of treatment was considered in the subjects' best interest due to safety concerns. ¨4Lack of efficacy ¨5Withdrawal of informed consent by patients (including withdrawal by patients themselves) ¨6Patients were lost to follow-up ¨7Other reasons: _____________ Number of treatments Week 1 Week 2 Week 3 Week 4 Total Number of times should be treated Actual number of treatments Case Report Form (CRF) review Statement 1、Confirm that the subject has signed the informed consent. 2、Confirm that the subject's name, mailing address and telephone number are true and complete. 3、Confirm that subjects meet the protocol inclusion criteria and do not meet the exclusion criteria. 4、Verify that treatment records are correct for subjects' group. 5、Confirm that all items in the study record are completely filled in, physical and chemical inspection results are complete, the original inspection report has been pasted on the "Test Sheet Paste page", and the "Report Form of Physical and chemical Inspection Results" has been correctly filled in. 6、Verify that all adverse events have been completed in the Adverse Event Form. Adverse events and physical and chemical examination data that were normal before and after treatment but could not be explained by deterioration of the disease were reviewed and followed up to normal 7、Confirm that subjects' withdrawal and loss of follow-up have been truthfully filled in the "Disengagement reason Form". 8、When it is confirmed that there is an error, mark the error value with “—”, write the correct value above the error, the modifier signs and notes the date, the reason for the change has been explained, and no original data has been covered. Signature of professional evaluator: _____________ Date of signing: 20 |__|__|year|__|__|month|__|__|day Quality control doctor's signature: _____________ Date of signing: 20 |__|__|year|__|__|month|__|__|day Principal investigator statement I reviewed all the records in this case report form page by page and item by item. I confirmed that these data were true, complete and accurate, consistent with the original data and in line with the design requirements of the study protocol. All the data recording work was done by me and my designee and we signed the researcher signature form. Principal investigator signature: _____________ Date of signing: 20 |__|__|year|__|__|month|__|__|day Check the adhesion of the test sheet: 1.Blood routine examination 2.Urine-RT. 3.Liver function Ⅰ. 4.Renal function Ⅰ. 5.B ultrasound prostate volume. 6.Bladder residual urine. 7.Urinary flow rate(Qmax).

Data Managemen Committee:

Yes

Publication information of the protocol/research results report
(name of the journal, volume, issue, pages, time; or website):

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