Clinical Trial

Comparing Prophylactic Intravenous Pethidine and Intrathecal Pethidine in Preventing Post Spinal Shivering in Caesarean Section

Recruiting Phase 3
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Record status
This record was last updated January 15, 2025 (before its estimated February 2025 completion). Its status may not reflect the trial's current state.
Summary
The goal of this clinical trial is to assess the effect of IV pethidine and intrathecal pethidine on the incidence, onset, duration, and intensity of shivering in females undergoing caesarean section. The main question it aims to answer is: which route is more efficacious in preventing shivering. Researchers will compare IV pethidine and intrathecal pethidine to see their effects on post spinal shivering, their effects on hemodynamic stability, nausea, vomiting, and sedation.
Trial Details
NCT Number NCT06775431
Lead Sponsor Alexandria University
Conditions Pregnant Women
Enrollment 86 participants
Start Date 2024-12-10
Primary Completion 2025-02 (estimated)
Study Completion 2025-03 (estimated)
Updated on ClinicalTrials.gov 2025-01-15