Pain Clinical Trial
Official title:
Study of Posterior Lumbar Plexus Block for Pain Relief After Hip Surgery
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.
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.
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