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Clinical Trial Summary

- To determine if the T-PTNS is not inferior in the short term (3 months) to one of the usual pharmacological treatments (Solifenacin) in the treatment of hyperactive bladder syndrome and with respect to the percentage of patients that improve 50% any of the 3 signs (Urinary frequency, diurnal / nocturnal frequency, urgency and urinary incontinence).

- To determine prognostic factors associated with insufficient improvement (less than 50% in the 3 main signs of hyperactive bladder syndrome (urinary frequency, urgency and urinary incontinence frequency) after treatment with T-PTNS and Solifenacin.


Clinical Trial Description

Patients will be randomized to receive the usual standard treatment with Solifenacin or treatment based on peripheral unilateral transcutaneous neuromodulation of the posterior tibial nerve . ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03468465
Study type Interventional
Source Fundacion para la Formacion e Investigacion Sanitarias de la Region de Murcia
Contact
Status Active, not recruiting
Phase Phase 4
Start date May 4, 2018
Completion date March 2019

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