Trial of Tibial Nerve Stimulation for Treating Sexual Dysfunction

Status Completed

Clinical Trial Summary

The purpose of this study is to understand the efficacy of PTNS versus a placebo in the treatment of female sexual dysfunction syndrome.

Clinical Trial Description

The goal of this study is to evaluate the efficacy of PTNS in treating patients with FSD. We will be recruiting 66 patients, who will be randomized (1:1) to either the PTNS group or the Sham group. The patients in the PTNS group will receive one PTNS treatment per week for 12 weeks. The patients in the Sham group will receive one sham treatment per week for 12 weeks. Patients in both groups will be asked to complete questionnaires before the start of the treatment, as well as after 12-weeks of treatment to assess the changes in the severity of their symptoms Aim 1: To evaluate the effect of percutaneous tibial nerve stimulation (PTNS), compared to a validated sham, on sexual functioning in women with female sexual dysfunction (FSD). Aim 2: To compare the effect of PTNS on lower urinary tract symptoms versus sexual functioning in patient with FSD. ;

Study Design

Related Conditions & MeSH terms

Female Sexual Dysfunction

Clinical Trial Details

NCT number	NCT04122703
Study type	Interventional
Source	Stony Brook University
Contact
Status	Completed
Phase	N/A
Start date	September 15, 2019
Completion date	June 30, 2023

View Details

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