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Maternal Satisfaction After Spinal Anesthesia for Cesarean Delivery

NCT07438171 · Status: NOT_YET_RECRUITING · Type: OBSERVATIONAL · Enrollment: 200

Last updated 2026-02-27

No results posted yet for this study

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

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

Sponsors & Collaborators

  • University of Novi Sad

    lead OTHER

Eligibility

Min Age
18 Years
Max Age
45 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2026-03-02
Primary Completion
2026-08-31
Completion
2026-09-01

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07438171 on ClinicalTrials.gov