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The effect of radiofrequency on improvement of vaginalaxity and loss of sexuality in wome

Not Applicable
Recruiting
Conditions
Vaginalaxity.
Female genital prolapse
Registration Number
IRCT20201006048949N1
Lead Sponsor
Mashhad University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Female
Target Recruitment
30
Inclusion Criteria

Age between 25-50 years
Having complaints of vaginal laxity
Not having breastfed within the the three months before the study
Sexual activity (vaginal sex at least once a month)
Normal Pap test result
Negative pregnancy test before entering the study

Exclusion Criteria

Pelvic organ prolapse has exceeded the hymenal ring (grade 3 and 4 prolapse)
Active sexually transmitted disease (Condylomata acuminata / herpes)
Chronic vulvar pain or vulvar dystrophy
Using known medications that affect sexual function (antihypertensive and psychotropic drugs / chemotherapeutic agents)
Daily use of anti-inflammatory drugs which can affect collagen in healing (ibuprofen / aspirin / steroids)
Chronic skin disorder including vulvar involvement
Medical problem that interferes with wound healing.
Thin rectovaginal septum
Under treatment for Hypoactive Sexual Desire Disorder (HSDD) or orgasmic disorder
Irritable bowel syndrome (IBS)

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Sexual function. Timepoint: Before the intervention, at months 1, 2, 3 during the study before each treatment session, and 3and 6 months after the intervention. Method of measurement: Female Sexual Function Index.;Vaginal laxity. Timepoint: Before the intervention, at months 1, 2, 3 during the study before each treatment session, and 3and 6 months after the intervention. Method of measurement: Vaginal Laxity Questionnaire.
Secondary Outcome Measures
NameTimeMethod
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