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Effects of fenghuaqinaqingfang (fenghuaqinaqingcha) prevention and treatment of binign prostatic hyperplasia clinical trial

Efficacy and Safety Study of fenghuaqinaqingfang (fenghuaqinaqingcha) prevention and treatment of benign prostatic hyperplasia (MAST): a Randomized Controlled Pilote Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IOR-16008151
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

benign prostatic hyperplasia

Interventions

test group:2 bag each time, 2 times a day
control group:1 piece each time, 1 time a day

Sponsors

Dongzhimen Hospital Beijing university of Chinese medicine
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
45 Years to 80 Years

Inclusion criteria

Inclusion criteria: (1) Aged 45-80 years, male; (2) More than 3 months duration; (3) Corresponding to diagnosis standards; (4) Maximum urinary flow rate <15ml/s; (5) Signed the informed consent; (6) Have stop drug treatment is at least 2 weeks before the visit.

Exclusion criteria

Exclusion criteria: (1) Allergies or allergic constitution; (2) Merge heart, cerebrovascular, liver, kidney and hematopoietic system and other serious primary diseases and psychiatric patients; (3) Severe nervous system disease, cervical stenosis, lumbar disc disease, pelvic or abdominal surgery, caused severe diabetic neurogenic bladder; (4) Bladder neck fibrosis, ureteral ridge between hypertrophy, verumontanum hypertrophy, urethral stricture cause dysuria; (5) Combination of urinary tract infection, urinary stones, men with prostate cancer; (6) Benign prostatic obstruction of invasive treatment failure; (7) Taking drugs may affect the function of bladder outlet; (8) Non-drug therapy indications.

Design outcomes

Primary

MeasureTime frame
QOL;IPSS;maximum urinary flow rate;

Secondary

MeasureTime frame
the residual urine;prostate volume;

Countries

China

Contacts

Public ContactQunchao Yan

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