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Determination of the effect of Vitex plant on the sexual satisfaction in Wome

Phase 3
Recruiting
Conditions
Description of health condition studied Sexual dysfunction.
Hypoactive sexual desire disorder
F52.0
Registration Number
IRCT20190703044086N1
Lead Sponsor
Rasht University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Female
Target Recruitment
126
Inclusion Criteria

All fertile women who referred for Pap smear and were healthy in gynecological and physical examinations and seeking treatment for the improvement and enhancement of sexual satisfaction

Exclusion Criteria

single, Pregnant and lactating, cannot read and write, Having a specific illness (thyroid problems, diabetes, psychiatric disorders, hyper-prolactonemia, liver problems, etc.) Stressful event in the last 6 months (death or disease of immediate family member, a major change in lifestyle) of any of the couples Mental problems (illness under the supervision or treatment of a physician) in each of the couples according to the woman's statement Treated for any sexual problems in each of the couples according to the woman's statement Alcohol or drug addiction in each of the couples according to the woman's statement Women whose husbands are unable to have normal sex (e.g., erectile dysfunction or premature ejaculation) Any illness in women, including abnormal bleeding, cervicitis and vaginitis without premenstrual tension and premenstrual syndrome. Taking vitamin supplements or hormonal pills like contraceptives

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Sexual Satisfaction. Timepoint: Before the intervention, 4, 8 and 12 weeks after the intervention. Method of measurement: Larson questionnaire.
Secondary Outcome Measures
NameTimeMethod
Medicinal effects. Timepoint: During and after medication. Method of measurement: Ask the patient.
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