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...