Status:
COMPLETED
Evaluation of Efficacy of Lumbar Plexus Bloc After Hip Surgery
Lead Sponsor:
University Hospital, Angers
Conditions:
Pain
Postoperative
Eligibility:
All Genders
18+ years
Phase:
NA
Brief 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 ev...
Detailed Description
Compare lumbar plexus block (randomized) * ropivacaine 0.475%, 0.4 ml/kg * saline 0.4 ml/kg . Each group includes 30 patients. Block performed preoperatively. Surgery under general anesthesia (sufe...
Eligibility Criteria
Inclusion
- adults
- ASA 1-3
Exclusion
- cognitive impairement
- ASA IV
Key Trial Info
Start Date :
September 1 2001
Trial Type :
INTERVENTIONAL
End Date :
March 1 2002
Estimated Enrollment :
60 Patients enrolled
Trial Details
Trial ID
NCT00150865
Start Date
September 1 2001
End Date
March 1 2002
Last Update
November 1 2017
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