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Effect of Cyproterone acetate in patients with Benign Prostatic Hypertrophy

Phase 3
Conditions
Benign Prostate Hypertrophy.
Enlarged prostate
Registration Number
IRCT20181106041572N1
Lead Sponsor
Mashhad University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Male
Target Recruitment
84
Inclusion Criteria

Patients with acute urinary retention complaints with initial diagnosis of BPH.

Exclusion Criteria

Prostate cancer
Urinary infections
Use of sympathomimetic drugs

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
rinary retention. Timepoint: checking of urinary retention immediately after removal of urinary catheter 7 days after starting of cyproterone acetate with ureteral catheter and re-examination one week and 4 weeks after it and follow up to 6 months later. Method of measurement: Observation.
Secondary Outcome Measures
NameTimeMethod
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