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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
France1 site in 1 countryChoose a country to see its sites
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

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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

This trial has no sites in United States.

It has sites in one country. Choose a country to see its sites.

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.

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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

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?

Contact the study team: see the registry record → Contacts and Locations

Print a page for my doctor

Data 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