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Clinical Trial Summary

The investigators conducted a prospective, randomized double-blind, placebo-controlled study based on a placebo technique to evaluate the efficacy of T-MPNS vs placebo in women with idiopathic OAB. The main questions aimed to be answered are: What are the effects of Transcutaneous Medial Plantar Nerve Stimulation (T-MPSS) on clinical parameters related to incontinence and quality of life compared to the placebo group in women with idiopathic overactive bladder (OAB)? Participants (n:40) with idiopathic OAB who meet the exclusion and inclusion criteria will be divided into 2 groups using a randomization table. The first group will receive T-MPSS (n:20) and the second group will receive placebo T-MPSS (n:20). Measurements will be performed twice in total, before and at the end of treatment (6th week).


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06390488
Study type Interventional
Source Pamukkale University
Contact Emre Bezmez, M.D.
Phone +905319902220
Email emrebezmez@gmail.com
Status Not yet recruiting
Phase N/A
Start date April 22, 2024
Completion date February 28, 2025

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