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The effect of oral evening primrose oil capsule on sexual function of wome

Phase 1
Conditions
Sexual dysfunction.
Sexual dysfunction not due to a substance or known physiological condition
Registration Number
IRCT20191127045517N1
Lead Sponsor
Tarbiat Modares University
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
60
Inclusion Criteria

Women over the age of 18 (age 18 is considered a good time for marriage) and before the age of pre-menopause (49 years).
Being Iranian and living in Tehran
Reading and Writing Persian Language
participants who had a monogamous husband during the study and at the beginning of it
Having sex in the last two months

Exclusion Criteria

Having a known underlying disease
Couples are addicted to drugs and alcohol
Having a history of pelvic surgery
pregnancy or breastfeeding
Having a mental illness
Sensitive to evening primrose oil
Taking drugs that affect sexual function
Have a stressful accident over the past month
Have a urinary tract infection
Having vaginitis, cervicitis, pelvic genital pain disorders, active sores or genital lesions that interfere with sexual intercourse (penetration)
Victims of rape
having the history of infertility

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Female sexual function. Timepoint: Evaluation of research units will be done 4 and 8 weeks after the intervention. Method of measurement: Female sexual function index.;Sexual Quality of Life. Timepoint: Evaluation of research unitswill be don 4 and 8 weeks after the intervention. Method of measurement: Sexual Quality of Life-Female (SQOL-F) questionnaire.
Secondary Outcome Measures
NameTimeMethod
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