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Ropivacaine LIA in Vaginal Prolapse Repair
NCT00769054Phase 4Completed
- Sponsor
- Copenhagen University Hospital - Hvidovre
- Start
- Oct 2008
- Primary completion
- Oct 2009
- Modality
- Orthosteric Ligands
- Countries
- 1
01
Overview
Phase 4, randomised, double-blind trial in vaginal prolapse comparing Ropivacaine with Placebo (2 arms). Primary endpoint: Postoperative Pain during rest, coughing and ambulation at 24 hours. Started Oct 2008; status: completed.
02
Drugs
ropivacaine
03
Conditions
vaginal prolapse
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