NCT07438171

Maternal Satisfaction After Spinal Anesthesia for Cesarean Delivery

Maternal Satisfaction Following Different Spinal Anesthesia Regimens for Elective Cesarean Delivery: a Prospective Observational Study

• Status: Not Yet Recruiting
• Phase: —
• Study type: Observational
• Enrollment: 200 (estimated)
• Sponsor: University of Novi Sad · Academic / Other
• Sex: Female
• Age: 18 Years – 45 Years
• Healthy volunteers: Not accepted

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.

Conditions

• Parturients
• Elective Cesarean Delivery

Interventions

Type	Name	Description
DRUG	Bupivacaine %0.5 (hyperbaric)	Only Bupivacaine %0.5 (hyperbaric) for spinal anesthesia
DRUG	Bupivacaine %0.5 (hyperbaric) and morphine	Combination of bupivacaine and morphine for spinal anesthesia
DRUG	Bupivacaine %0.5 (hyperbaric), morphine and fentanyl 15	Bupivacaine %0.5 (hyperbaric) , morphine and fentanyl 15 mcg for spinal anesthesia
DRUG	Bupivacaine, morphine and fentanyl 20	Bupivacaine, morphine and fentanyl 20 mcg for spinal anesthesia

Timeline

• Start date: 2026-03-02
• Primary completion: 2026-08-31
• Completion: 2026-09-01
• First posted: 2026-02-27
• Last updated: 2026-02-27