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Effect of new combined medication Young Prostate on clinical symptoms in patients with benign prostate hypertrophy and overactive bladder

Phase 3
Recruiting
Conditions
Benign prostate hypertrophy.
Benign neoplasm of prostate
D29.1
Registration Number
IRCT20120215009014N386
Lead Sponsor
Hamedan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Male
Target Recruitment
64
Inclusion Criteria

Age of 40 to 65 years
Benign prostate hypertrophy
Overactive bladder

Exclusion Criteria

History of prostate surgery

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Sexual desire. Timepoint: Before the intervention and 3 and 6 months after that. Method of measurement: By taking history.;Prostate size. Timepoint: Before the intervention and 3 and 6 months after that. Method of measurement: Using ultrasonography.
Secondary Outcome Measures
NameTimeMethod
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