the effect of saffron(crocus sativus) on female sexual function in reproductive age
Phase 3
- Conditions
- female sexual dysfunction.other sexual dysfunction, not caused by organic disorder or disease
- Registration Number
- IRCT201206265912N5
- Lead Sponsor
- ursing & Midwifery Care Research Center
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 80
Inclusion Criteria
Inclusion criteria: Women age 18-39 years; Iranian; Being married; No pregnancy
Lack of breastfeeding; The ability of Reading and writing; Lack of diseases affecting sexual function in person or her spouse; Lack of using drugs influence sexual function in person or her spouse; Lack of sexual dysfunction in her spouse;Not be multi partner her spouse; Not used hormonal drugs in recent months; Not used drugs in the past 6 months; Lack of allergy to herbal medicine; Lack of participation in other similar studies.
Exclusion criteria: Lack of volunteers willing to continue taking drug; The occurrence of pregnancy during the study; Symptoms of allergy medication;
Stressful life event.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Desire. Timepoint: Before intervention/ 4 week after intervention/8week after intervention. Method of measurement: Standardized questionnaire FSFI.;Excitement. Timepoint: Before intervention/ 4 week after intervention/ 8 week after intervention. Method of measurement: Standardized questionnaire FSFI.;Lubricaton. Timepoint: Before intervention/ 4 week after intervention/ 8 week after intervention. Method of measurement: Standardized questionnaire FSFI.;Orgasem. Timepoint: Before intervention/ 4 week after intervention/ 8 week after intervention. Method of measurement: Standardized questionnaire FSFI.;Sexual Satisfaction. Timepoint: Before intervention/ 4 week after intervention/ 8 week after intervention. Method of measurement: Standardized questionnaire FSFI.;Dysparonia. Timepoint: Before intervention/ 4 week after intervention/ 8 week after intervention. Method of measurement: Standardized questionnaire FSFI.
- Secondary Outcome Measures
Name Time Method