Effect of Stinging Nettle (Urtica dioica L.) extract in patients with Benign Prostate Hyperplasia
Phase 2
Completed
- Conditions
- Benign Prostate Hyperplasia.Enlarged prostate
- Registration Number
- IRCT20170430033730N4
- Lead Sponsor
- Qazvin University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Male
- Target Recruitment
- 60
Inclusion Criteria
Patients with benign prostatic hyperplasia
Exclusion Criteria
Patients who use anticoagulant
Diabetic patients
Patients with hypo and/or hyperthyroidism
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method International Prostate Symptom Score (I-PSS). Timepoint: At the beginning of the study and 12 weeks after the intervention. Method of measurement: Standard questionnaire.;Insulin. Timepoint: At the beginning of the study and 12 weeks after the intervention. Method of measurement: calculation based on standard formula.
- Secondary Outcome Measures
Name Time Method