Status:
UNKNOWN
Propofol for Prophylaxis of Morphine Induced Pruritis in Caesarean Section
Lead Sponsor:
Assiut University
Conditions:
Pruritus Caused by Drug
Eligibility:
FEMALE
20-40 years
Phase:
PHASE3
Brief 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...
Eligibility Criteria
Inclusion
- The study is scheduled for women undergoing elective caesarean section under spinal anesthesia.
- The subject is ≥ 20 years and ≤ 40 years.
- No obvious abnormalities in preoperative ECG, blood routine, electrolytes, and other tests.
- ASA class 1-2.
Exclusion
- 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
Key Trial Info
Start Date :
January 1 2024
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
March 1 2025
Estimated Enrollment :
200 Patients enrolled
Trial Details
Trial ID
NCT06188546
Start Date
January 1 2024
End Date
March 1 2025
Last Update
January 3 2024
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