Transverse Abdominal Plane Block for Caesarean

Université NAZI BONI

Status: Completed

Conditions: Caesarean Section; Pain

Treatments: Other: TAP block

Study type: Interventional

Funder types: Other

Identifiers

NCT05588752

INSSA 2

Details and patient eligibility

About

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

Enrollment: 100 patients

Sex: All

Ages: 18+ years old

Volunteers: Accepts Healthy Volunteers

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

Trial design

Primary purpose: Other

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

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100 participants in 2 patient groups

group 1

No Intervention group

Description:

will receive at induction of spinal anesthesia 100 µg of morphine

group 2

Experimental group

Description:

No morphine in spinal anesthesia but will receive a bilateral TAP block with 20 ml of Bupivacaine 0.25% and dexamethasone 4 mg in the same syringe on each side

Treatment:

Other: TAP block