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Clinical study for Gui-Huang decoction based on sore-ulcer-resolving method in the treatment of chronic prostatitis and Chronic pelvic pain syndrome

Clinical study for Gui-Huang decoction based on sore-ulcer-resolving method in the treatment of chronic prostatitis and Chronic pelvic pain syndrome

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900026966
Enrollment
Unknown
Registered
2019-10-27
Start date
2019-10-26
Completion date
Unknown
Last updated
2019-10-28

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

Conditions

Chronic prostatitis

Interventions

Control group:Tamoxine hydrochloride sustained release capsule

Sponsors

Xiyuan Hospital of China Academy of Chinese Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: 1. Age 18-50 years old; 2. Those who meet the diagnostic criteria of CP/CPPS Western medicine; 3. Comply with the criteria of TCM syndrome differentiation of damp heat syndrome; 4. The course of disease is more than 3 months; 5. At least 2 weeks after stopping treatment at the time of treatment.

Exclusion criteria

Exclusion criteria: 1. Allergic constitution or allergic to the drug; 2. Bacterial culture or mycoplasma, chlamydia and other pathogenic microorganisms positive; 3. With prostate hyperplasia, prostate cancer patients; 4. Combined with other genitourinary diseases and other diseases; 5. Combined Severe cardiovascular and cerebrovascular, liver and kidney dysfunction and hematopoietic system diseases; 6. Unable to cooperate, such as mental patients.

Design outcomes

Primary

MeasureTime frame
NIH-CPSI;

Countries

China

Contacts

Public ContactGao Qinghe

Xiyuan Hospital, China Academy of Chinese Medical Sciences

gaoqinghe1949@126.com+86 13581968952

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 18, 2026