MedPath

Effectiveness of biofeedback for sexual function in women with vaginismus

Not Applicable
Recruiting
Conditions
Vaginismus.
Vaginismus
N94.2
Registration Number
IRCT20200710048069N2
Lead Sponsor
Esfahan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Female
Target Recruitment
32
Inclusion Criteria

Married women who have not yet succeeded in intercourse through penetration.
Age range from 18 to 45 years.
Primary vaginismus grade 2 to 4 (according to the Lamont classification).
The patient's desire for treatment.

Exclusion Criteria

Pregnancy
Secondary vaginismus
The presence of hymen structural disorders
Congenital vaginal disorders
Vulvodynia
Infection
Menopause
Pelvic pathology (such as malignant masses, fractures, etc.)
Psychological diseases
Spouse's sexual disorders (erectile dysfunction, premature ejaculation, etc.)
History of urogenital surgeries (such as labiaplasty, hymenectomy, etc.)

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Female Sexual Function (including desire, arousal, lubrication, orgasm, satisfaction, and pain). Timepoint: The Female Sexual Function Index questionnaire is completed by the patient at the beginning, at the end of 6 weeks of treatment, and also one month after the end of treatment. Method of measurement: Female Sexual Function Index questionnaire.
Secondary Outcome Measures
NameTimeMethod
© Copyright 2025. All Rights Reserved by MedPath