Clinical Research Directory
Browse clinical research sites, groups, and studies.
Maternal Satisfaction After Spinal Anesthesia for Cesarean Delivery
Sponsor: University of Novi Sad
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.
Official title: Maternal Satisfaction Following Different Spinal Anesthesia Regimens for Elective Cesarean Delivery: a Prospective Observational Study
Key Details
Gender
FEMALE
Age Range
18 Years - 45 Years
Study Type
OBSERVATIONAL
Enrollment
200
Start Date
2026-03-02
Completion Date
2026-09-01
Last Updated
2026-02-27
Healthy Volunteers
No
Conditions
Interventions
Bupivacaine %0.5 (hyperbaric)
Only Bupivacaine %0.5 (hyperbaric) for spinal anesthesia
Bupivacaine %0.5 (hyperbaric) and morphine
Combination of bupivacaine and morphine for spinal anesthesia
Bupivacaine %0.5 (hyperbaric), morphine and fentanyl 15
Bupivacaine %0.5 (hyperbaric) , morphine and fentanyl 15 mcg for spinal anesthesia
Bupivacaine, morphine and fentanyl 20
Bupivacaine, morphine and fentanyl 20 mcg for spinal anesthesia