Status:
UNKNOWN
Pain Score and Opioid Consumption of Index and Previous Cesarean Delivery
Lead Sponsor:
Prince of Songkla University
Conditions:
Pain
Postoperative
Eligibility:
FEMALE
18+ years
Brief Summary
Postoperative pain after cesarean delivery is common and affects on both mothers and children. The goals of this retrospective observational study aim to predict pain score and opioid consumption of ...
Detailed Description
The authors will review the medical records of recruited participants for demographic data as well as pain scores and opioid consumption of index cesarean delivery and previous cesarean delivery.
Eligibility Criteria
Inclusion
- Patients who had at least 2 cesarean deliveries
- Patients received spinal anesthesia and intrathecal morphine for cesarean delivery
- Patients received postoperative pain control as per standard protocol
Exclusion
- Patients with chronic pain prior to cesarean delivery
- Unable to give pain score
- Receiving general anesthesia for cesarean delivery
- Receiving postoperative pain control beyond the standard protocol
- Patients with multiple pregnancy, placenta abruption, placenta accrete, postpartum hemorrhage
- Patients with psychotic disorder
Key Trial Info
Start Date :
January 1 2024
Trial Type :
OBSERVATIONAL
Allocation :
ESTIMATED
End Date :
December 1 2025
Estimated Enrollment :
416 Patients enrolled
Trial Details
Trial ID
NCT06178458
Start Date
January 1 2024
End Date
December 1 2025
Last Update
December 28 2023
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