Maternal Satisfaction After Spinal Anesthesia for Cesarean Delivery
Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexFemale
Age18-45
SponsorUniversity of Novi Sad
About this trial
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.
Eligibility criteria
Qualifiers
None
Disqualifiers
None
Trial design
Treatments tested in this trial
- Bupivacaine %0.5 (hyperbaric)
- Bupivacaine %0.5 (hyperbaric) and morphine
- Bupivacaine %0.5 (hyperbaric), morphine and fentanyl 15
- Bupivacaine, morphine and fentanyl 20
Treatment groups
No treatment groups listed
Locations
Sponsors and collaborators
Source ClinicalTrials.gov