Investigating the effect of royal jelly on Sexual Dysfunction due to the use of selective serotonin reuptake inhibitors
Phase 2
Recruiting
- Conditions
- post SSRI sexual dysfunction.Major depressive disorder, single episode
- Registration Number
- IRCT20191207045632N1
- Lead Sponsor
- Sabzevar University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 60
Inclusion Criteria
patients with any psychological disease that need SSRI
patients with sexual dysfunction after using SSRI
patients aged between 20 to 45
Exclusion Criteria
patients who do not use SSRI regularly
patients who had sexual dysfunction history before using SSRI
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Sexual function. Timepoint: at the beginning of the study ( before intervention), week 2, week 4, week 6 and week 8. Method of measurement: Arizona sexual experience scale (ASEX) and the changes in sexual functioning questionnaire (CSFQ).
- Secondary Outcome Measures
Name Time Method