Ultrasound Guided TAPB vs Surgical TAPB With Bupivacaine in Cesarean Section

NCT05750992 · tracked via the Priya Life Science Egypt tracker

Sponsor

Al-Azhar University

Phase

Not applicable

Started

2023-04-10

Last updated

2026-01-06

Condition(s) studied

Cesarean SectionUltrasound Guided Transversus Abdominis Plane BlockSurgical Transversus Abdominis Plane BlockBupivacaineAcute Pain

Investigational drug(s) / intervention(s)

surgical TAP blockUS guided TAP block

surgical TAP block: performed by 40 ml of 0.25% bupivacaine (10 ml 0.5% bupivacaine bilaterally diluted with 10cc normal saline and 100 μg of fentanyl), the total volume was divided equally and administered bilaterally by the surgeon.

US guided TAP block: performed by 40 ml of 0.25% bupivacaine (10 ml 0.5% bupivacaine bilaterally diluted with 10cc normal saline and 100 μg of fentanyl), the total volume was divided equally and administered bilaterally.

Study summary

The aim of this study is to compare Surgical Transversus abdominis plane block and Ultrasound guided transversus abdominis plane block (TAPB) as a postoperative analgesic regimen in female patients undergoing elective cesarean delivery.

Eligibility

Sex

FEMALE

Min age

21 Years

Max age

35 Years

Healthy volunteers

Inclusion Criteria: * Full term pregnant women * Older than 21 years of age * Had elective cesarean section with Pfannenstiel incision. Exclusion Criteria: * Patients with cesarean section using different surgical incision * History of addiction \[including opioids and benzodiazepines\] * Allergy to the anesthetic analgesia * Psychological disorders * Coagulopathies * Infection at the block injection site.

Primary outcome measure(s)

Time to perform block. — 1 hour postoperatively
The time taken to perform the block will be recorded by an independent observer.

Trial sites (1)

Facility	City	Region	Status
Kohaf	Cairo	Egypt	Recruiting

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05750992 on ClinicalTrials.gov ↗ ← All trials in Egypt