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the effect of saffron(crocus sativus) on female sexual function in reproductive age

the effect of saffron(crocus sativus) on female sexual function in reproductive age

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT201206265912N5
Enrollment
80
Registered
2013-10-13
Start date
2013-07-23
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

female sexual dysfunction. other sexual dysfunction, not caused by organic disorder or disease

Interventions

Intervention 1: Saffron Ex tract/ Oral Capsul 15mg/ Twice a day/ For 8 week. Intervention 2: Placebo/ No Action/Oral Placebo Capsul/ Twice a day for 8 week.
Treatment - Drugs
Placebo
Saffron Ex tract/ Oral Capsul 15mg/ Twice a day/ For 8 week
Placebo/ No Action/Oral Placebo Capsul/ Twice a day for 8 week

Sponsors

Nursing & Midwifery Care Research Center
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 39 Years

Inclusion criteria

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

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
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.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMandana Mirmohama Ali Ei

Nursing &Midwifery Faculty - Tehran University Of Medical Science

mirmohamad1@yahoo.com+98 21 6692 7171

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026