Functional Outcomes of the Miami Pouch Continent Cutaneous Urinary Diversion: A Quality of Life Study
Key facts
- Who runs it
- Hospices Civils de Lyon
- Where
- Pierre-Bénite, FranceSee the site
- Trial code
- Status
- Not yet recruiting
- People taking part
- 35 people, planned
- Starts
- 16 Nov 2026
- Expected to end
- 16 Apr 2027
- Type of study
- Observational
- Treatments tested
- Patient reported outcome measures
- 24-Hour Stomal Pad Test
- Record updated
- 12 November 2026
Who can take part
- Age
- 18 years and older
- Sex
- Women and men
- Healthy volunteers
- Cannot take part
The registry criteria, word for word
Show all 8 criteriaShow less
Who can take part
- Adult patients aged 18 years or older
- Miami Pouch continent cutaneous urinary diversion performed at Lyon Sud Hospital (HCL) between January 2015 and December 2025
- Minimum postoperative follow-up of 6 months
- No opposition to participation in the study
Who cannot take part
- Patient deceased at time of study contact
- Patient unreachable or unavailable after three contact attempts
- Opposition to participation or to personal data processing
- Postoperative follow-up of less than 6 months
Where in France
- Hopital Lyon SudPierre-Bénite, FranceContact: Théo ARBER, MDNo longer taking part
About the trial
What the trial wants to find out
The Miami Pouch is a continent cutaneous urinary diversion using the plicated right colon and the ileocecal valve as a catheterizable continent stoma. Despite its long history, functional outcomes remain poorly reported, with no consensus on continence definition or standardized assessment tools.
Read full original descriptionShow less
This single-center cross sectional cohort study evaluates functional outcomes in patients who underwent Miami Pouch urinary diversion at Hôpital Lyon Sud (Hospices Civils de Lyon, France) between 2015 and 2025. Patients were identified through institutional medical coding (PMSI) and contacted by telephone to complete validated patient-reported outcome measures.
The primary objective is to assess stomal continence using the International Consultation on Incontinence Questionnaire - Short Form (ICIQ-SF).
Hypothesis: The Miami Pouch provides acceptable long-term stomal continence with limited impact on digestive function.
The group in the trial
- Miami pouch
Adult patients who underwent Miami Pouch continent cutaneous urinary diversion at the Urology Department of Hôpital Lyon Sud (HCL) between 2015 and 2025, with a minimum postoperative follow-up of 6 months
Treatment: Patient reported outcome measures and 24-Hour Stomal Pad Test
Questions to ask the study team
- How often do I need to come in, and for how long each time?
- Are travel costs paid?
- Can I keep my own doctor?
- What happens if I want to stop?
Contact the study team: see the registry record → Contacts and Locations
Print a page for my doctorData and sources
- Registry record
- Listed on ClinicalTrials.gov.
- Official title
- Functional Urinary and Digestive Outcomes After Miami Pouch: A Quality-of-Life Study (MIADIG)
- Record updated
- 12 November 2026