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
This trial does not accept healthy volunteersQualifiers
None
Disqualifiers
None
Trial population
Pregnant women, 18- 45 y old, with singleton pregnancy, scheduled for elective cesarean delivery
Trial design
Design model
Cohort
Time perspective
Prospective
Treatments tested in this trial
Bupivacaine %0.5 (hyperbaric)
DrugOnly Bupivacaine %0.5 (hyperbaric) for spinal anesthesia
Bupivacaine %0.5 (hyperbaric) and morphine
DrugCombination of bupivacaine and morphine for spinal anesthesia
Bupivacaine %0.5 (hyperbaric), morphine and fentanyl 15
DrugBupivacaine %0.5 (hyperbaric) , morphine and fentanyl 15 mcg for spinal anesthesia
Bupivacaine, morphine and fentanyl 20
DrugBupivacaine, morphine and fentanyl 20 mcg for spinal anesthesia
Treatment groups
No treatment groups listed
Trial outcomes
Primary outcomes
1
Maternal satisfaction with provided analgesia during first 24 h following cesarean delivery
Time frame
24 hoursSecondary outcomes
1
The need for rescue analgesics
Time frame
24 hoursLocations
Sponsors and contacts
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Source ClinicalTrials.gov
This trial is not recruiting at the moment. You can still explore other options: