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Clinical Trials/NCT06556381
NCT06556381CompletedNot Applicable

The Efficacy of Ultrasound-guided Transversus Abdominis Plane ( TAP) Block Versus Standard Analgesic Protocol for Postoperative Analgesia After Elective, Cesarean- Section Delivery- A Randomize Controlled Trial

Qassim University1 site in 1 country100 target enrollmentStarted: April 1, 2024Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
100
Locations
1
Primary Endpoint
Pain Score

Study Overview

Brief Summary

Relief from pain is part of the fundamental human right to health. (1) However, available evidence indicates an increasingly detailed understanding of the pathophysiology of pain and general inadequacy of its treatment.

Detailed Description

Background: Relief from pain is part of the fundamental human right to health. (1) However, available evidence indicates an increasingly detailed understanding of the pathophysiology of pain and general inadequacy of its treatment.

Rationale: Assessment and Improving the Pain Management Modality

Study objectives: In this study, determined the efficacy of TAP block in patients undergoing cesarean section.

Methods:

This study is a cross-sectional study. It is a multi-centric study as it was conducted in different Governmental hospitals.

Study Design

Study Type
Interventional
Allocation
Non Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to 50 Years (Adult)
Sex
Female
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Age: 20-50 years
  • •Patients of >50 kg or <100 kg weight.
  • •Urgency: Elective, Emergent and Urgent cases

Exclusion Criteria

  • •Patients of <50 kg or >100 kg weight
  • •Any contraindication to any of anesthesia medications
  • •Patient unable to understand numeric rating scale (NRS)

Arms & Interventions

Group A,

Experimental

women who received TAP block.

Intervention: TAP block (Procedure)

Group B

Active Comparator

Received Usual modality of analgesics (Paracetamol, Tramadol, and Pethidine).

Intervention: TAP block (Procedure)

Outcomes

Primary Outcomes

Pain Score

Time Frame: 24 hours

NRS

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Mohammed Abaalkhayl

Associate Proffesor

Qassim University

Study Sites (1)

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