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Completed

NCT Number: NCT05588752

Transverse Abdominal Plane Block for Caesarean

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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Key information

Conditions

Caesarean Section; Pain Neurologic Manifestations Pain Pain, Postoperative Pathologic Processes Pathological Conditions, Signs and Symptoms Postoperative Complications Signs and Symptoms

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

CHU Souro Sanou

Bobo-Dioulasso, Houet, Burkina Faso

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

TAP Block

Other

TAP block under ultrasound

Primary outcomes

  1. 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

  1. Proportion of mild pain at rest in the first 24 postoperative hours

    Time frame: Hours 24 postoperative

    The numerical pain score at rest

  2. Proportion of mild pain on mobilization in the first 48 postoperative hours

    Time frame: Hours 48 postoperative

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

  3. Proportion of nausea-vomiting postoperative during the first 48 hours

    Time frame: Hours 48 postoperative

    At each passage of the nurses

  4. Proportion of maternal satisfaction during the first 48 hours postoperatively

    Time frame: Hours 48 postoperative

    The simple numerical score

Interested in participating?

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Sponsors and collaborators

Lead sponsor

Université NAZI BONI

Other

Registry information

Official study title

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

Important dates

Study start
2022
Primary completion
2023
Study completion
2023
First posted
Oct 20, 2022
Registry last updated
Sep 7, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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