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Study identifier: NCT07574437 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

At-Home Bowel Stimulation

Condition: Post-Operative Ileus (POI)  ·  Sponsor: The Cleveland Clinic

PhaseN/A
Planned participants34
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

Postoperative ileus (POI) is a common complication after ileostomy closure and is associated with patient discomfort, delayed return of bowel function, prolonged hospital stay, and increased healthcare costs. One proposed contributor to POI is prolonged inactivity of the bowel segment distal to the ileostomy prior to restoration of intestinal continuity. Previous studies, including a multicenter randomized controlled trial, have shown that preoperative bowel stimulation of the defunctionalized intestine can reduce rates of POI and shorten length of hospital stay. However, these interventions were performed in outpatient or hospital settings and required specialized nursing support. This single-center, prospective interventional study aims to evaluate the feasibility and clinical impact of a patient-performed, at-home bowel stimulation program prior to ileostomy closure. Participants will perform daily bowel stimulation sessions at home for 3 weeks before surgery, following an initial supervised session. The primary objective is to assess feasibility, defined as successful completion of at least 6 of 9 at-home stimulation sessions by more than 75% of participants. Secondary outcomes include return to normal bowel function and length of hospital stay. Exploratory outcomes include postoperative bowel function, quality of life, and patient satisfaction. Study outcomes will be compared with a retrospective cohort of patients who previously underwent ileostomy closure without at…

This description comes directly from the study's public registry record.

Talk to the study team

Marylise Boutros, MD  ·  954-659-5278  ·  BOUTROM3@ccf.org

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Locations (1)

Cleveland Clinic FloridaWeston, Florida, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT07574437