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
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
DOUBLE
Enrollment
41
Hospital Universitari de Bellvitge
L'Hospitalet de Llobregat, Barcelona, Spain
Hospital Vall d'Hebron
Barcelona, Spain
Tibial nerve stimulation efficacy measured by LARS score
Time frame: 1 month
Tibial nerve stimulation efficacy measured by LARS score
Time frame: 3 months
Tibial nerve stimulation efficacy measured by LARS score
Time frame: 6 months
Tibial nerve stimulation efficacy measured by LARS score
Time frame: 12 months
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