Pain, Postoperative
Conditions
Keywords
ropivacaine, posterior lumbar plexus block, hip arthroplasy, analgesia, postoperative
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 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.
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 (sufentanil, propofol, atracurium ; maintenance : sevoflurane and nitrous oxide in O2. Sufentanil added peroperatively as clinically needed. Postoperative evaluation of pain (VAS, by an independant blind observer) as first endpoint, and also morphine consumption via PCA device. Adverse effects (nausea, vomiting, etc) recorded Follow-up : 24h. Expectation : sizeable reduction of pain with block, of duration.
Interventions
Sponsors
Study design
Eligibility
Inclusion criteria
* adults * ASA 1-3
Exclusion criteria
* cognitive impairement * ASA IV
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| decrease of postoperative pain | — |
Secondary
| Measure | Time frame |
|---|---|
| decrease in morphine consumption | — |
| duraration of analgesic effect | — |