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Decades of data: does this bladder surgery stand the test of time for spinal cord injury?

NCT ID NCT04936217

Knowledge-focused Sponsor: Centre Hospitalier Universitaire de Nīmes Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This completed study from France reviewed the long-term results of a surgery called continent cutaneous urinary diversion in 70 spinal cord injury patients. The surgery creates a new way to drain urine through the belly when patients cannot use a catheter normally. Researchers collected medical records and conducted phone surveys to see how well the procedure worked over time and what complications occurred.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
continent cutaneous urinary diversion (Mitrofanoff/Yang-Monti/Casale procedure)
What this could lead to
If successful, this could confirm that this surgical technique is a reliable long-term option for bladder management in spinal cord injury patients who cannot use a catheter through the urethra.
What could go wrong
This is a small, completed observational study with no control group, so results may not apply to all patients. It only collects existing data and does not test a new treatment.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Participants

70 people

The number who actually took part.

Started

Aug 2020

Finished

Dec 2022

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Who is studied

All patients who have suffered a spinal cord injury, operated on between April 2004 and October 2017 at Nîmes University Hospital.

Ages

17 years and older

Sex

Anyone

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: Specific inclusion criteria for the study : * no history of continuous cystostomy in another centre * a follow-up \> 24 months, * a continent cutaneous urinary diversion for a spinal cord injury. General inclusion criteria : * Patient affiliated to or beneficiary of a health insurance scheme. * Adult patient (≥18 years of age) and under 85 years of age. Exclusion Criteria: * Criteria for non-inclusion specific to the study : * All urinary incontinence outside of medullary waiting period. * A history of continuous cystostomy in another centre. * A follow-up of less than 24 months, * a continent cutaneous urinary diversion for a neurological pathology other than spinal cord injury. General criteria for non-inclusion : * Patient in a period of exclusion determined by another study. * Patient for whom it is impossible to give enlightened information. * Patient under legal protection, guardianship or curatorship. * Patient unable to express consent

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Conditions

The condition(s) this trial relates to.

spinal cord injury Urinary Bladder, Neurogenic

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Neurogenic bladder Spinal cord injuries Urinary diversion

Contacts and locations

Locations

  • Nîmes University Hospital

    Nîmes, Gard, 30029, France

More trials for these conditions

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