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Clinical Trial Summary

The purpose of this study is to compare the efficacy, duration of motor block until return to normal function in the non-operated leg after the start of injection, of ropivacaine 5 mg/ml and bupivacaine 5 mg/ml when used for spinal anaesthesia in patients undergoing unilateral lower limb surgery.


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double-Blind, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT00358280
Study type Interventional
Source AstraZeneca
Contact
Status Completed
Phase Phase 3
Start date April 2006
Completion date September 2006

See also
  Status Clinical Trial Phase
Completed NCT00991627 - Different Approaches to Maternal Hypotension During Cesarean Section Phase 4
Completed NCT00921102 - Atropine to Prevent Nausea and Vomiting After Spinal Anesthesia for Caesarean Section Phase 4