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Efficacy of Trans Abdominis Plane Block for Post Cesarean Delivery Analgesia

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

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06556381
Enrollment
100
Registered
2024-08-16
Start date
2024-04-01
Completion date
2026-04-30
Last updated
2026-05-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Analgesia

Keywords

Pain, cesarean delivery

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.

Interventions

PROCEDURETAP block

Women will receive TAP block.

Sponsors

Qassim University
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 50 Years
Healthy volunteers
No

Inclusion criteria

1. Age: 20-50 years 2. Patients of \>50 kg or \<100 kg weight. 3. Urgency: Elective, Emergent and Urgent cases

Exclusion criteria

1. Patients of \<50 kg or \>100 kg weight 2. Any contraindication to any of anesthesia medications 3. Patient unable to understand numeric rating scale (NRS)

Design outcomes

Primary

MeasureTime frameDescription
Pain Score24 hoursNRS

Countries

Saudi Arabia

Contacts

PRINCIPAL_INVESTIGATORMohammed Abaalkhayl, MD

Qassim University

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 28, 2026