Clinical Performance of the GYNECARE PROLIFT + M* Pelvic Floor Repair System as a Device for Pelvic Organ Prolapse
Summary
The registered summary isn't in our current data snapshot. Read it on the ClinicalTrials.gov record ↗. Why? →
Investigators
The overall officials registered on this study. Names that resolve to a findmyKOL profile link to it; the rest are shown as registered.
- David Robinson, MD
Ethicon, Inc.
Study Director
A profile link is shown only when the registered name resolves to a person record with a confident, namesake-checked match; ambiguous names stay unlinked.
Sites
8 registered facilities, with the per-site recruitment status where the registry publishes one. ClinicalTrials.gov does not publish per-site enrollment counts.
- Sint Lodewijkstraat 78
Genk, Belgium
- Chru de Lille
Lille, France
- Drt Krankenhaus
Chemnitz, Germany
- Martin Luther University
Halle, Germany
- Kreiskrankenhaus
Hamelin, Germany
- Universitatsklinik Tubingen
Tübingen, Germany
- St. Marien-Hospital
Vechta, Germany
- Reinier de Graaf Gasthuis
Delft, Netherlands
Site investigator names are published by ClinicalTrials.gov only while a study recruits, so completed studies list sites without them.
Drugs studied
No drug or biological interventions are in our data for this study — it may test a procedure, device or behavioral intervention, or the intervention list isn't in our current snapshot. See the registry record ↗. Why? →
Registration & key dates
Registry attributes as recorded on the ClinicalTrials.gov study record.
- Start
- 30 Apr 2008
- Primary completion
- 30 Nov 2009
- Completion
- 31 Dec 2011
- Last update posted
- 6 May 2014
- Registered enrollment
- 126
- Registry id
- NCT00833001
Source: ClinicalTrials.gov, via the CTTI AACT database, data as of 12 Jul 2026. Registry facts are shown as registered by the study sponsor; findmyKOL does not interpret them.