Evaluation of radiofrequency therapy effectiveness on sexual dysfunctio

Not Applicable

• Conditions: Sexual dysfunction.; Sexual dysfunction, unspecified

• Registration Number: IRCT20160531028187N2
• Lead Sponsor: Shahid Beheshti University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 7 February 2023

Recruitment & Eligibility

• Status: Complete
• Sex: Female
• Target Recruitment: 74

Inclusion Criteria

Sexually active postmenopausal women
Patients with malignancy 3 months after completing treatment

Exclusion Criteria

Hormone therapy (systemic or topical) or other treatments for sexual dysfunction (such as moisturizers)
Mild sexual dysfunction (score above 28 according to the questionnaire)
Patients with active or recurrent genital tract infection (such as herpes or candida infection)
People infected with HIV
Urinary tract infection
Pelvic reconstructive surgery
Having a pacemaker
Having intra-uterine device
Pregnancy
Breast feeding
Skin diseases
Not signing the informed consent form

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Dyspareunia. Timepoint: Before the intervention and three months after the intervention. Method of measurement: Female Sexual Function Index Scoring questionnaire.;Sexual Desire. Timepoint: Before the intervention and three months after the intervention. Method of measurement: Female Sexual Function Index Scoring questionnaire.;Sexual Arousal. Timepoint: Before the intervention and three months after the intervention. Method of measurement: Female Sexual Function Index Scoring questionnaire.;Sexual Satisfaction. Timepoint: Before the intervention and three months after the intervention. Method of measurement: Female Sexual Function Index Scoring questionnaire.;Sexual Lubrication. Timepoint: Before the intervention and three months after the Intervention. Method of measurement: Female Sexual Function Index Scoring questionnaire.;Orgasm. Timepoint: Before the intervention and three months after the intervention. Method of measurement: Female Sexual Function Index Scoring questionnaire.