drugset / Trial / NCT00150865

Evaluation of Efficacy of Lumbar Plexus Bloc After Hip Surgery

NCT00150865 ↗

Completed 60 enrolled University Hospital, Angers
RandomizedSingle-groupDouble-blindTreatment

Summary

Compare lumbar plexus block with ropivacaine 0.475%, 0.4 ml/kg to saline. Each group randomized, includes 30 patients. block performed preoperatively Surgery under general anesthesia. Postoperative evaluation of pain (VAS) as first endpoint, and also morphine consumption via PCA device. Follow-up : 24h. Expectation : sizeable reduction of pain with block, of duration.

Timeline

Start
2001-09
Primary completion
—
Completion
2002-03

Drugs

EvaluationDrugModalityDoseRoute
Subject Ropivacaine Other / unclassified 0.475 % —

Indications

No indication recorded.