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Effects of compound sabal berry tablets on benign prostatic hyperplasia: an open-label, multicenter clinical trial in Chinese population

Effects of compound sabal berry tablets on benign prostatic hyperplasia: an open-label, multicenter clinical trial in Chinese population

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800015211
Enrollment
Unknown
Registered
2018-03-14
Start date
2009-05-01
Completion date
Unknown
Last updated
2018-03-19

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

Conditions

benign prostatic hyperplasia

Interventions

Case series:compound sabal berry tablets

Sponsors

West China Hospital of Sichuan
Lead Sponsor

Eligibility

Sex/Gender
Male

Inclusion criteria

Inclusion criteria: 1. aged > 50 years; 2. the international prostate symptom score (IPSS) score = 13 and the quality of-life (QoL) score = 3; 3. the volume (V) of prostate > 25 mL; 4. Qmax 4 mL/s to 15 mL/s; 5. residual urine (RU) < 200 mL; 6. serum prostate specific antigen (PSA) = 4ng/mL; 7. voluntary participation; and 8. drugs with an effect on micturition function or other forbidden drugs should be stopped at least 2 weeks prior to entry the study. Patients were allowed to enter in this study unless they fulfilled all the above inclusion criteria.

Exclusion criteria

Exclusion criteria: Patients with urination disorder that caused by other diseases, such as prostate cancer, bladder malignancy, neurogenic bladder, urinary dysfunction, bladder stones, recurrent urinary tract infection, recurrent gross hematuria, or large diverticulum, were excluded from the study. In addition, patients who had previous prostate or urethra surgery or patients with other diseases, such as poorly controlled diabetes, cardiovascular disease, and hepatic or renal dysfunction, were excluded from the study.

Design outcomes

Primary

MeasureTime frame
(IPSS);

Countries

China

Contacts

Public ContactQiang Wei

Department of Urology, West China Hospital of Sichuan

liuchuan_03@126.com+86 18144340551

Outcome results

None listed

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