U.S., Aug. 13 -- ClinicalTrials.gov registry received information related to the study (NCT07761884) titled 'Early Implementation of Sacral Neuromodulation in Patients With Low Anterior Resection Syndrome.' on July 27.

Brief Summary: 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.

Study Start Date: Aug., 2026

Study Type: INTERVENTIONAL

Condition: Low Anterior Resection Syndrome (LARS)

Intervention: DEVICE: Sacral neuromodu...