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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05588752
Other study ID # INSSA 2
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date October 20, 2022
Est. completion date February 20, 2023

Study information

Verified date September 2023
Source Université NAZI BONI
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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


Recruitment information / eligibility

Status Completed
Enrollment 100
Est. completion date February 20, 2023
Est. primary completion date January 20, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility 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

Study Design


Related Conditions & MeSH terms


Intervention

Other:
TAP block
TAP block under ultrasound

Locations

Country Name City State
Burkina Faso CHU Souro Sanou Bobo-Dioulasso Houet

Sponsors (1)

Lead Sponsor Collaborator
Université NAZI BONI

Country where clinical trial is conducted

Burkina Faso, 

Outcome

Type Measure Description Time frame Safety issue
Primary Proportion of mild pain on mobilization in the first 24 postoperative hours The numerical pain score after moving from a lying position to a sitting position Hours 24 postoperative
Secondary Proportion of mild pain at rest in the first 24 postoperative hours The numerical pain score at rest Hours 24 postoperative
Secondary Proportion of mild pain on mobilization in the first 48 postoperative hours The numerical pain score after moving from a lying position to a sitting position Hours 48 postoperative
Secondary Proportion of nausea-vomiting postoperative during the first 48 hours At each passage of the nurses Hours 48 postoperative
Secondary Proportion of maternal satisfaction during the first 48 hours postoperatively The simple numerical score Hours 48 postoperative
See also
  Status Clinical Trial Phase
Completed NCT04847024 - Parecoxib vs. Dexketoprofen for the Management of Pain After Cesarean Section. N/A