Propofol for Prophylaxis of Morphine Induced Pruritis in Caesarean Section
Status:
Not yet recruiting
Trial end date:
2025-03-01
Target enrollment:
Participant gender:
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.