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Clinical Trial Summary

The aim of this study is to evaluate the efficiency of the Neuroestimulation of the Posterior Tibial Nerve for the treatment of this syndrome.

A multicentric, prospective, randomized study will be performed in patients affected with severe LARS symptoms. Patients will be randomized in two groups:

1. Control group- placebo

2. Treatment group: neuroestimulation of the posterior tibial nerve


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02517853
Study type Interventional
Source Hospital Universitari Vall d'Hebron Research Institute
Contact
Status Completed
Phase N/A
Start date February 1, 2016
Completion date August 7, 2019

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