Saffron and decrease of sexual dysfunction induced by fluoxeti
Phase 2
- Conditions
- Sexual dysfunction.Lack or loss of sexual desire
- Registration Number
- IRCT138711121556N3
- Lead Sponsor
- Tehran University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Male
- Target Recruitment
- 40
Inclusion Criteria
Inclusion Criteria: at least 4 weeks usage of fluoxetin before study, do not use any psychotherapeutics except Selective Seretonin Reuptake Inhibitors, lack of chronic and organic disorders including cardiovascular diseases, informed consent.
Exclusion Criteria
substance dependence, organic disorders, other psychiatric comorbidity including biploar disorder, use of psychotropic drugs.
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Score of international index of Erectile Function. Timepoint: every two weeks. Method of measurement: use of international index of Erectile Function.
- Secondary Outcome Measures
Name Time Method