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Analysis of the therapeutic effect of Qianlie suppository on patients with type IIIB prostatitis with damp heat and stasis syndrome and mechanism research based on PINK1/PARKIN pathway

Analysis of the therapeutic effect of Qianlie suppository on patients with type IIIB prostatitis with damp heat and stasis syndrome and mechanism research based on PINK1/PARKIN pathway

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2024000606
Enrollment
Unknown
Registered
2024-10-25
Start date
2024-11-20
Completion date
Unknown
Last updated
2024-11-11

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

Conditions

Chronic prostatitis.

Interventions

Treatment group:Qianlianshuan in combination with Tamsulosin Hydrochloride Extended-release Capsules.
Control group:Tamsulosin Hydrochloride Extended-release Capsules

Sponsors

Henan Provincial Hospital of Traditional Chinese Medicine (Second Affiliated Hospital of Henan University of Traditional Chinese Medicine)
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: (1) Age between 18 and 50 years old; (2) Meeting the Western medical diagnostic criteria for type IIIB prostatitis; (3) Syndrome differentiation in Traditional Chinese Medicine consistent with damp-heat obstruction and blood stasis; (4) NIH-CPSI total score between 15 and 43 inclusive; (5) Disease course of more than 3 months; (6) Those who have received other treatments before the trial must discontinue any medication for at least 2 weeks;

Exclusion criteria

Exclusion criteria: (1) Patients with allergic constitution allergy to this medication or those who cannot tolerate the drug; (2) Those with concurrent urinary tract infections acute prostatitis prostate hyperplasia urinary system stones urethral stricture prostate cancer or other diseases; (3) Patients with severe heart brain blood vessel diseases liver kidney dysfunction hypotension mental illness or other diseases; (4) Those who plan to conceive during the medication period or within 1 month after the end of medication; (5) Individuals who have participated in other clinical trials within the past 3 months.

Design outcomes

Primary

MeasureTime frame
NIH-CPSI Score;

Secondary

MeasureTime frame
Prostate fluid levels of inflammatory cytokines (TNF-a IL-8 IL-1ß);Pain scoring;Prostatic fluid lecithin body count;

Countries

China

Contacts

Public ContactYucong Jia

Henan Provincial Hospital of Traditional Chinese Medicine (Second Affiliated Hospital of Henan University of Traditional Chinese Medicine)

rain19860731@163.com15136101679

Outcome results

None listed

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