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Clinical Trial Summary

the goal of this randomized clinical trial is to find the optimum sub hypnotic dose of iv propofol that prevents the incidence of itching induced from intrathecal morphine used in spinal anesthesia in caesarean section operation. the main questions it aim to answer are the number of patients complained of pruritus in the first 24 hours post operative period and the severity of the pruritus. participants will be divided into 4 groups. 1st group receives 0 mg of propofol , 2nd receives 10 mg , 3rd receives 20 mg and the 4th receives 30 mg.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06188546
Study type Interventional
Source Assiut University
Contact Sohila K Hassan, MBBCH
Phone 201010328326
Email khaledsohila@gmail.com
Status Not yet recruiting
Phase Phase 3
Start date January 1, 2024
Completion date March 1, 2025