|
Main
|
|
Note: This record shows only the 20 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
|
Register:
|
ClinicalTrials.gov |
|
Last refreshed on:
|
17 October 2012 |
|
Main ID: |
NCT00150865 |
|
Date of registration:
|
07/09/2005 |
|
Primary sponsor: |
|
|
Public title:
|
Evaluation of Efficacy of Lumbar Plexus Bloc After Hip Surgery
|
|
Scientific title:
|
Study of Posterior Lumbar Plexus Block for Pain Relief After Hip Surgery |
|
Date of first enrolment:
|
September 2001 |
|
Target sample size:
|
60 |
|
Recruitment status: |
Completed |
|
URL:
|
http://clinicaltrials.gov/show/NCT00150865 |
|
Study type:
|
Interventional |
|
Study design:
|
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Double-Blind, Primary Purpose: Treatment
|
|
|
Contacts
|
|
Name:
|
ibrahim okais, MD |
|
Address:
|
|
|
Telephone:
|
|
|
Email:
|
|
|
Affiliation:
|
Clinique St Leonard |
|
|
Name:
|
laurent beydon, MD |
|
Address:
|
|
|
Telephone:
|
|
|
Email:
|
|
|
Affiliation:
|
University Hospital, Angers |
| |
|
Key inclusion & exclusion criteria
|
Inclusion Criteria:
- adults
- ASA 1-3
Exclusion Criteria:
- cognitive impairement
- ASA IV
Age minimum:
18 Years
Age maximum:
N/A
Gender:
Both
|
|
Health Condition(s) or Problem(s) studied
|
|
Pain
|
|
Postoperative
|
|
Intervention(s)
|
|
Drug: ropivacaine
|
|
Primary Outcome(s)
|
|
decrease of postoperative pain
|
|
Secondary Outcome(s)
|
|
decrease in morphine consumption
|
|
duraration of analgesic effect
|
|
Source(s) of Monetary Support
|
|
Please refer to primary and secondary sponsors
|
|