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NOT YET RECRUITING
NCT07761884
NA

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

Sponsor: Hospital Universitari Vall d'Hebron Research Institute

View on ClinicalTrials.gov

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.

Official title: Early Implementation of Sacral Neuromodulation in Patients With Low Anterior Resection Syndrome: a Randomized, Multicenter, Prospective, Open-label, Pragmatic Study.

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

40

Start Date

2026-08

Completion Date

2030-02

Last Updated

2026-08-12

Healthy Volunteers

No

Interventions

DEVICE

Sacral neuromodulation

Sacral neuromodulation implantation within 120 days from discharge following rectal surgery or bowel reconstruction (ileostomy closure)

Locations (1)

Vall d'Hebron Barcelona Hospital Campus

Barcelona, Catalonia, Spain