Transverse Abdominal Plane Block for Caesarean

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

100 participants

Study Classification

INTERVENTIONAL

Study Start Date

2022-10-20

Study Completion Date

2023-02-20

Brief Summary

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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

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Detailed Description

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Conditions

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Caesarean Section; Pain

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Patients admitted for caesarean under spinal anesthesia were randomized according to the sealed envelope method into two groups. Group 1 received 100 µg of morphine intrathecally at induction and group 2 a bilateral TAP block at the end of cesarean section with 20 ml of bupivacaine 0.25% and dexamethasone 4 mg in the same syringe on each side.

Primary Study Purpose

OTHER

Blinding Strategy

SINGLE

Participants

Study Groups

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group 1

will receive at induction of spinal anesthesia 100 µg of morphine

Group Type NO_INTERVENTION

No interventions assigned to this group

group 2

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

Group Type EXPERIMENTAL

TAP block

Intervention Type OTHER

TAP block under ultrasound

Interventions

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TAP block

TAP block under ultrasound

Intervention Type OTHER

Eligibility Criteria

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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

Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes