Skip to main content
Clinical Trials/NCT05588752
NCT05588752
Completed
Not Applicable

Efficacy of Transverse Abdominal Plane Block (TAP Block) With Bupivacaine and Dexamethasone for the Management of Post-cesarean Pain at the CHU Sourô Sanou (CHUSS) in Bobo-Dioulasso

Université NAZI BONI1 site in 1 country100 target enrollmentOctober 20, 2022

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Caesarean Section; Pain
Sponsor
Université NAZI BONI
Enrollment
100
Locations
1
Primary Endpoint
Proportion of mild pain on mobilization in the first 24 postoperative hours
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

Cesarean sectionis a commonly performed major surgical procedure that results in significant postoperative pain. The objective of this study was to evaluate the effectiveness in the management of post-cesarean pain at the CHU Souro Sanou of Bobo-Dioulasso

Registry
clinicaltrials.gov
Start Date
October 20, 2022
End Date
February 20, 2023
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Université NAZI BONI
Responsible Party
Principal Investigator
Principal Investigator

Ismael Guibla

Clinical doctor

Université NAZI BONI

Eligibility Criteria

Inclusion Criteria

  • Adult parturients (≥ 18 years old) awaiting caesarean section under spinal anesthesia
  • ASAI, ASAII

Exclusion Criteria

  • Lack of informed consent,
  • Parturients with cognitive disorders,
  • Parturients with notion of chronic pain,
  • Allergy to local anesthetics,
  • Morphine allergy
  • Parturients not understanding pain assessment scores

Outcomes

Primary Outcomes

Proportion of mild pain on mobilization in the first 24 postoperative hours

Time Frame: Hours 24 postoperative

The numerical pain score after moving from a lying position to a sitting position

Secondary Outcomes

  • Proportion of mild pain at rest in the first 24 postoperative hours(Hours 24 postoperative)
  • Proportion of mild pain on mobilization in the first 48 postoperative hours(Hours 48 postoperative)
  • Proportion of nausea-vomiting postoperative during the first 48 hours(Hours 48 postoperative)
  • Proportion of maternal satisfaction during the first 48 hours postoperatively(Hours 48 postoperative)

Study Sites (1)

Loading locations...

Similar Trials