A Prospective Pilot Study to Assess the Efficacy of BOTOX-A in Patients With Low Anterior Resection Syndrome (LARS>20) and Refractory Medical Treatment After Rectal Resection

Clinical trial NCT04991688 · TERMINATED

Trial details

NCT number: NCT04991688
Sponsor: University Hospital, Bordeaux
Status: TERMINATED
Phase: Phase 2
Study type: INTERVENTIONAL

Low Anterior Resection Syndrome (LARS>20)Refractory Medical Treatment After Rectal Resection

Start date: 2021-09-01
Primary completion: 2023-01-07
Enrollment: 11

View on ClinicalTrials.gov

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