Abstract
Materials and Method: This is a randomized double blind controlled clinical trial which was approved by the ethics committee of Iran University of Medical Sciences. Fifty patients (25 patients in each groups) in ASA class 1 or 2 which were selected for surgery on lower limbs, entered into the study. The patients were randomly allocated in two groups and received following regimens: CP (spinal anesthesia with combination of clonidine 0.75 µgr/kg and pethidine 0.75 mg/kg) and B (spinal anesthesia with bupivacaine 0.5%, 15 mg).
Results: The onset time of sensory block on T10 in group CP (5.9±1.6 min) was significantly less than group B (9.2±2.3 min) [p<0.001]. The time to complete motor block in group CP (38.8±5.7 min) was significantly longer than group B (19.6±4.7 min) [p<0.001]. The time to the first analgesic request was significantly longer in the group CP (11.6±2 h) than the group B (6±0.8 h) [p<0.001]. Mean drop in the systolic blood pressure in group CP (22.6%±2.4%) was significantly more than group B (11%±4.3%) (p<0.001).
Conclusion: It is recommended to use bupivacaine for anesthesia in operations on pelvis and lower limbs but it is better to co-administer clonidine and pethidine in patients who must be avoided from raising blood pressure and heart rate and with less than two hours operation time
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