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NCT02899520: ReedPerinee

Evaluation of Programs of Reeducation for Urinary Incontinence in Woman

Terminated NA Last updated 3 January 2020
What this trial tests

NA trial testing Reference method in Urinary Incontinence in 60 participants. Terminated before completion.

Timeline
10 November 2014
Primary endpoint
18 October 2019
18 October 2019

Quick facts

Lead sponsorHopital Foch
PhaseNA
StatusTerminated
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposetreatment
Enrollment60
Start date10 November 2014
Primary completion18 October 2019
Estimated completion18 October 2019
Sites1 location across France

Drugs / interventions tested

Conditions studied

Sponsor

Hopital Foch — full company profile →

Who can join

Adults 18 to 75, female only, with Urinary Incontinence. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The objective of this study is to compare two methods of pelvic floor muscle training: reference method versus CMP ® method ( (Connaissance et Maîtrise de Périnée : Knowledge and Control of Perineum)

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Electrical stimulation with non-implanted devices for stress urinary incontinence in women.
    Stewart F, Berghmans B, Bø K, Glazener CM. · · 2017 · cited 45× · PMID 29271482 · DOI 10.1002/14651858.cd012390.pub2

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Other recruiting trials for Urinary Incontinence

Currently open trials in the same condition.

Other Hopital Foch trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT02899520.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing