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Taking people in FranceNo phase

Studies bladder sensation and overactive bladder in people with multiple sclerosis

Checks how bladder feelings during filling relate to overactive bladder in adults with multiple sclerosis.

Plain-language title generated from the registry record
Registry title: Clinical and Urodynamic Assessment of Bladder Sensation in Multiple Sclerosis

Key facts

Where
Paris, FranceSee the site

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 18 and 99 years old?

Source: NCT05772637, who can take part

Where in France

  • Hôpital TenonParis, FranceTaking people

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?
Print a page for my doctor

Trial details

Who runs it
Assistance Publique - Hôpitaux de Paris
Trial code
NCT05772637
Record updated
5 March 2026
Original description
The aim of the study is to assess the association between bladder sensations progression during bladder filling and severity of Overactive bladder (OAB) in patients with multiple sclerosis.Read full original descriptionShow less

Clinical and Urodynamic Assessment of Bladder Sensation in Multiple Sclerosis

The aim of the study is to assess the association between bladder sensations progression during bladder filling and severity of Overactive bladder (OAB) in patients with multiple sclerosis.

Inclusion: Age ≥ 18; MS according to the 2017 Mac Donald diagnostic criteria; Bladder disorders supposedly related to MS; Indication to perform urodynamics; No current medication for bladder disorders; Able to understand and right in French; Affiliated to the "Securite sociale" or "Couverture Medicale Universelle (CMU)", or equivalent organism.

Exclusion: Treatment with antimuscarinics, alpha blockers, beta3 adrenergic, or tibial nerve stimulation in the past 15 days, or with botulinic toxin injection in the past 6 months; Previous lower urinary tract surgery; Other associated neurological disease; Legal protection; Pregnancy or breastfeeding mother; MS relapse during the past month; Genuine stress incontinence related to postpartum; Inability to use the analogic device due to motor, sensory or ataxic disabilities.

ClinicalTrials.gov NCT05772637