Maternal Satisfaction After Spinal Anesthesia for Cesarean Delivery

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

Status

Not yet recruiting

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT07438171

Enrollment

200

Registered

2026-02-27

Start date

2026-03-02

Completion date

2026-09-01

Last updated

2026-02-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Parturients, Elective Cesarean Delivery

Keywords

Maternal satisfaction, Spinal anesthesia, cesarean delivery, postcesarean analgesia

Brief 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.

Interventions

DRUGBupivacaine %0.5 (hyperbaric)

Only Bupivacaine %0.5 (hyperbaric) for spinal anesthesia

DRUGBupivacaine %0.5 (hyperbaric) and morphine

Combination of bupivacaine and morphine for spinal anesthesia

DRUGBupivacaine %0.5 (hyperbaric), morphine and fentanyl 15

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

DRUGBupivacaine, morphine and fentanyl 20

Bupivacaine, morphine and fentanyl 20 mcg for spinal anesthesia

Study design

Observational model

COHORT

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

FEMALE

Age

18 Years to 45 Years

Healthy volunteers

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. -

Design outcomes

Primary

Measure	Time frame
Maternal satisfaction with provided analgesia during first 24 h following cesarean delivery	24 hours

Secondary

Measure	Time frame
The need for rescue analgesics	24 hours

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 28, 2026