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NCT Number: NCT07438171

Maternal Satisfaction After Spinal Anesthesia for Cesarean Delivery

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.

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Key information

Conditions

Parturients Elective Cesarean Delivery

Age range

18 year–45 year

Sex eligibility

Female

Study type

Observational

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Parturients for elective cesarean delivery, ASA, status II and III, age between 18 and 45 years, singleton pregnancy, able to provide inform consent. -

Exclusion criteria

Refuse to participate in the study, spinal anesthesia refused, known drug allergies to drugs included in the study, multiple pregnancy, preterm gestation, skin lesion at the beck, severe maternal comorbidities, chronic opioid use and chronic pain. -

Treatment and study plan

Bupivacaine %0.5 (hyperbaric)

Drug

Only Bupivacaine %0.5 (hyperbaric) for spinal anesthesia

Bupivacaine %0.5 (hyperbaric) and morphine

Drug

Combination of bupivacaine and morphine for spinal anesthesia

Bupivacaine %0.5 (hyperbaric), morphine and fentanyl 15

Drug

Bupivacaine %0.5 (hyperbaric) , morphine and fentanyl 15 mcg for spinal anesthesia

Bupivacaine, morphine and fentanyl 20

Drug

Bupivacaine, morphine and fentanyl 20 mcg for spinal anesthesia

Primary outcomes

  1. Maternal satisfaction with provided analgesia during first 24 h following cesarean delivery

    Time frame: 24 hours

Secondary outcomes

  1. The need for rescue analgesics

    Time frame: 24 hours

Sponsors and collaborators

Lead sponsor

University of Novi Sad

Other

Registry information

Official study title

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

Important dates

Study start
2026
Primary completion
2026
Study completion
2026
First posted
Feb 27, 2026
Registry last updated
Feb 27, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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