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Effects of fenghuaqinaqingfang (fenghuaqinaqingcha) prevention and treatment of chronic prostatitis clinical trial

Efficacy and Safety Study of fenghuaqinaqingfang (fenghuaqinaqingcha) prevention and treatment of chronic prostatitis: a Randomized Controlled Pilote Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IOR-16008150
Enrollment
Unknown
Registered
2016-03-25
Start date
2016-04-08
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

chronic prostatitis

Interventions

test team:2 bags each time, 2 times a day
control team:1 piece each time, 1 time a day

Sponsors

Dongzhimen Hospital Beijing university of Chinese medicine
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
20 Years to 50 Years

Inclusion criteria

Inclusion criteria: (1) Conform to the standard diagnosis of chronic prostatitis; (2) More than 3 months duration; (3) Ranging in age from 20 to 50 years old men (including 20, 55 years of age); (4) Voluntary participation in the clinical research and fill out the informed consent; (5) Have stop drug treatment is at least 2 weeks before the visit.

Exclusion criteria

Exclusion criteria: (1) Do not accord with standard of the diagnosis of chronic prostatitis; (2) Acute prostatitis, benign prostatic hyperplasia, neurogenic bladder, prostate cancer, epididymitis, urinary calculi, urinary tract malformation, urethral stricture and severe disease such as neurosis patients; (3) Combination of heart, brain, liver and hematopoietic system, etc. Patients with severe primary diseases; (4) Allergic constitution, or drug allergy to the variety of the patients; (5) Can't cooperate with treatment, such as mental illness.

Design outcomes

Primary

MeasureTime frame
chronic prostatitis symptom index;EPS;

Countries

China

Contacts

Public ContactYan Qunchao

Guangzhou Hongyun Medical Scientific and Technological Co., Ltd

yqunchao@163.com+86 13902283853

Outcome results

None listed

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