Clinical Trial

Maternal Satisfaction After Spinal Anesthesia for Cesarean Delivery

Not Yet Recruiting
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Summary
The goal of this observational study is to evaluate the impact of four different spinal anesthesia regimens on maternal satisfaction following cesarean delivery. The main questions this study aims to answer are: * Primary outcome: Patient satisfaction with the provided analgesia during the first 24 hours postoperatively. * Secondary outcome: The need for rescue analgesics. Participants will complete a specially designed questionnaire 24 hours after cesarean delivery.
Trial Details
NCT Number NCT07438171
Lead Sponsor University of Novi Sad
Conditions Parturients, Elective Cesarean Delivery
Enrollment 200 participants
Start Date 2026-03-02
Primary Completion 2026-08-31 (estimated)
Study Completion 2026-09-01 (estimated)
Updated on ClinicalTrials.gov 2026-02-27