Clinical trial Recruiting at 1 site Interventional Ages 21 to 35 Women only

Comparing two methods of pain relief after cesarean delivery

Official title: Ultrasound Guided Transversus Abdominis Plane Block (TAPB) vs Surgical TAPB With Bupivacaine for Acute Pain Control in Cesarean Section: A Randomized Clinical Trial

Run by Al-Azhar University · NCT05750992 · Data updated 2026-11-12

This study is testing which pain relief method, Surgical Transversus Abdominis Plane Block or Ultrasound Guided TAPB, works better for women having a cesarean delivery.

Quick facts

Study typeInterventional
Ages21 Years to 35 Years
SexWomen only
Enrollment50 (estimated)
SponsorAl-Azhar University
Academic / other
Locations1 site (Cairo)
StatusRecruiting
StartedApril 10, 2023
Main results expectedDecember 30, 2026
Study endsDecember 30, 2026
Registry record updatedJanuary 6, 2026
Trial IDNCT05750992 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates for this study are full-term pregnant women over 21 years of age scheduled for elective cesarean sections with a Pfannenstiel incision.

Probably not a fit

Patients with a history of addiction, allergies to anesthetics, psychological disorders, coagulopathies, or infections at the injection site may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This study aims to compare the effectiveness of Surgical Transversus Abdominis Plane Block (TAPB) and Ultrasound Guided TAPB as postoperative pain management techniques for women undergoing elective cesarean sections. Given the high rates of cesarean deliveries in Egypt, the study seeks to determine which method provides better analgesia while minimizing risks associated with traditional techniques. The research will involve full-term pregnant women over 21 years of age who are scheduled for elective cesarean delivery with a specific incision type. The study will assess pain relief outcomes and potential complications associated with each method.

Why it matters

Potential benefit: If successful, this study could lead to improved pain management techniques for women undergoing cesarean sections, enhancing their recovery experience.

How similar studies have gone: Other studies have shown promising results with ultrasound-guided techniques, suggesting potential advantages over traditional methods, though this specific comparison may be novel.

Who can join: the full rules

Show full inclusion / exclusion criteria
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.

Where it's running

  • Kohaf
    Cairo, Egypt
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.