Skip to main content
Clinical Trials/NCT06089200
NCT06089200CompletedPhase 2

Comparison of Post-operative Analgetics With Transversus Abdominis Block and Spinal Morphine for Post-Caesarean Section: A Randomised Trial Study

Universitas Padjadjaran2 sites in 1 country44 target enrollmentStarted: February 23, 2023Last updated:
Conditions

Trial Snapshot

Phase
Phase 2
Status
Completed
Enrollment
44
Locations
2
Primary Endpoint
Length of time the patient needed the first additional opioid analgesics

Study Overview

Brief Summary

The goal of this randomized controlled trial is to compare the effect of TAP block vs spinal morphine for post caesarean section analgesics. The main questions it aims to answer are:

  • Which post op analgesic method works better for patients who underwent caesarean section
  • The number of additional opioid needed

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Triple (Participant, Care Provider, Investigator)

Eligibility Criteria

Ages
18 Years to 45 Years (Adult)
Sex
Female
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Indicated for caesarean section as assessed by Obstetricians
  • Consented to be included in the study

Exclusion Criteria

  • Allergy history
  • Spinal converted to general anesthesia

Outcomes

Primary Outcomes

Length of time the patient needed the first additional opioid analgesics

Time Frame: 24 hours post operative

Total need for additional opioids

Time Frame: 24 hours post operative

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (2)

Loading locations...

Similar Trials

TAP Block vs Spinal Orphine for... | Clinical Trial