Propofol for Prophylaxis of Morphine Induced Pruritis in Caesarean Section

• Status: Not yet recruiting
• Trial end date: 2025-03-01
• Target enrollment: 0
• Participant gender: Female

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.

• Phase: Phase 3
• Accepts Healthy Volunteers?: Accepts Healthy Volunteers

Details

• Lead Sponsor: Assiut University
• Treatments: Propofol

Criteria

Inclusion Criteria:

1. The study is scheduled for women undergoing elective caesarean section under spinal anesthesia.

2. The subject is ≥ 20 years and ≤ 40 years.

3. No obvious abnormalities in preoperative ECG, blood routine, electrolytes, and other tests.

4. ASA class 1-2.

Exclusion Criteria:

• Patients who had a known allergy to propofol, morphine, or bupivacaine.

• Those with preexisting pruritus caused by pregnancy, a coexisting skin disorder, or other pruritogenic systemic diseases.

• Patients with a contraindication to spinal anaesthesia

• Failed block

• Need of extra sedation intra-operative

• Positive history for asthma or COPD.

• Patient refusal