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Clinical Trial Summary

This interventional double-blind randomized controlled study was carried out on 60 cases underwent elective caesarean section delivery, they were divided into 2 groups; patients were randomly allocated into two equal groups; Group M: received intrathecal 150 microgram morphine in a 0.5 ml volume, mixed with 10 mg of hyperbaric bupivacaine 0.5 % in a 2 ml volume (total volume 2.5 ml). Group B: received intrathecal 10 mg hyperbaric bupivacaine 0.5% 2ml volume + 0.5 saline (Total volume 3ml) and at the end of surgery patient received bilateral TAP block with 20 ml volume of 0.25% bupivacaine on each side.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05331781
Study type Interventional
Source Sohag University
Contact
Status Completed
Phase N/A
Start date January 1, 2020
Completion date February 1, 2022

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