Maternal Satisfaction After Spinal Anesthesia for Cesarean Delivery

N/ANot Yet RecruitingNCT07438171

University of Novi Sad200 enrolled

Overview

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.

Study Type

OBSERVATIONAL

Enrollment

200

Conditions

Parturients Elective Cesarean Delivery

Interventions

Bupivacaine %0.5 (hyperbaric)DRUG

Only Bupivacaine %0.5 (hyperbaric) for spinal anesthesia

Bupivacaine %0.5 (hyperbaric) and morphineDRUG

Combination of bupivacaine and morphine for spinal anesthesia

Bupivacaine %0.5 (hyperbaric), morphine and fentanyl 15DRUG

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

Eligibility

Sex: FEMALEMin age: 18 YearsMax age: 45 Years

Medical Language ↔ Plain English

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. -

Outcomes

Primary Outcomes

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

Time frame: 24 hours

Secondary Outcomes

The need for rescue analgesics

Time frame: 24 hours

Data from ClinicalTrials.gov

This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.