The effect of bupropion on the improvement of sexual side effects caused by SSRI use
Phase 2
Recruiting
- Conditions
- Sexual dysfunction.Sexual dysfunction not due to a substance or known physiological condition
- Registration Number
- IRCT20151022024650N2
- Lead Sponsor
- Tabriz University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Female
- Target Recruitment
- 60
Inclusion Criteria
Patients under SSRI treatment for at least three consecutive months;
having sexual dysfunction for at least the last two months;
married and sexually active;
Age range 15-55 years;
stable vital signs.
Exclusion Criteria
The presence of digestive problems such as severe nausea and vomiting and SSRI intolerance;
The presence of concurrent chronic liver or kidney disease;
The presence of any anatomical problem of the reproductive system;
The existence of any severe or relatively severe hormonal disorder;
Absence of pregnancy;
Lack of breastfeeding;
Non-participation in the study.
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Measuring sexual satisfaction. Timepoint: Once a Month. Method of measurement: Hudson's Standardized Sexual Satisfaction Questionnaire (ISS).;Measuring sexual performance. Timepoint: Once a Month. Method of measurement: Rozen Standardized Women's Sexual Performance Questionnaire (FSFI).
- Secondary Outcome Measures
Name Time Method