Early Implementation of Sacral Neuromodulation in Patients With Low Anterior Resection Syndrome.

A randomized, prospective, multicenter, open-label, pragmatic pilot study of patients with Low Anterior Resection Syndrome treated early (\<120 days after discharge following intestinal bypass reconstruction) with sacral nerve root neuromodulation, compared with another group receiving personalized conservative treatment as performed in routine clinical practice.

NCT Number	NCT07761884
Lead Sponsor	Hospital Universitari Vall d'Hebron Research Institute
Conditions	Low Anterior Resection Syndrome (LARS)
Enrollment	40 participants
Start Date	2026-08
Primary Completion	2029-08 (estimated)
Study Completion	2030-02 (estimated)
Updated on ClinicalTrials.gov	2026-08-12