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Canceled by the investigator. Clinical study on the treatment of benign prostatic hyperplasia of kidney qi deficiency type with Qianlong Shutong prescription

Clinical study on the treatment of benign prostatic hyperplasia of kidney qi deficiency type with Qianlong Shutong prescription

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300070957
Enrollment
Unknown
Registered
2023-04-27
Start date
2022-02-01
Completion date
Unknown
Last updated
2023-06-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Prostatic hyperplasia

Interventions

control group:Tamsulosin Hydrochloride Sustained Release Capsule
treatment group:Qianlong Shutong Formula+Tamsulosin Hydrochloride Sustained Release Capsule

Sponsors

Ruikang Hospital Affiliated to Guangxi University of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
50 Years to 75 Years

Inclusion criteria

Inclusion criteria: ? Meet the diagnostic criteria of traditional Chinese medicine or western medicine; ? Patients aged 50-75 years; ? International Prostate Symptom Score (IPSS) for mild patients (IPSS<7) and moderate patients (7 = IPSS = 20); ? Number of nocturnal urination = 3 times; ? The symptoms of benign prostatic hyperplasia appear for more than three months, and the residual urine volume measured is greater than 50ml; ? Patients who have good compliance, can adhere to medication, and receive regular follow-up visits; ? Those who have signed an informed consent form and voluntarily joined the study;

Exclusion criteria

Exclusion criteria: ? Those who do not meet the inclusion criteria; ? There are also other urogenital diseases, such as prostatitis, neurogenic bladder, urethral stricture, etc.; ? Having undergone prostate surgery or other special treatment; ? Patients with various chronic diseases, psychiatric patients, and liver and kidney dysfunction; ? Allergic to observation drug; ? Those who are allergic to this drug or do not use it according to regulations, unable to judge the efficacy or incomplete information, which may affect the efficacy or safety judgment; ? Persons who have not participated in other clinical trials

Design outcomes

Primary

MeasureTime frame
International Prostate Symptom Score;TCM syndrome score;Determination of residual urine volume in the bladder;Quality of life index score;

Secondary

MeasureTime frame
Liver and renal function;

Countries

china

Contacts

Public Contactze-chao ZHANG

Ruikang Hospital Affiliated to Guangxi University of Chinese Medicine

edwardbangong@163.com+86 17671793908

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026