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Search / Trial NCT06765772

Combined Ultrasound Guided Bilateral Rectus Sheath and Erector Spinae Plain Blocks Versus Erector Spinae Plain Block for Intra and Postoperative Analgesia in Elective Abdominoplastic Surgeries. a Randomized Controlled Double Blinded Trial.

Launched by CAIRO UNIVERSITY · Jan 3, 2025

Trial Information

Current as of June 26, 2025

Recruiting

Keywords

Rectus Sheath Block Erector Spinae Plane Block

ClinConnect Summary

This clinical trial is looking at two different methods for managing pain during and after elective abdominoplasty surgeries, which are procedures to reshape the abdominal area. The main question is whether using a combination of two specific types of pain relief techniques—called bilateral rectus sheath and erector spinae plane blocks—works better than just using one of them alone, the erector spinae plane block. The goal is to see if the combined method can help patients feel less pain while using less morphine, a strong pain medication.

To participate in this trial, you need to be between the ages of 21 and 60, and have a specific health status (ASA I or II), which means you're generally healthy or have mild health issues. Unfortunately, if you're outside this age range, have a serious health condition, or are allergic to the medications used in the study, you won't be eligible. If you join the study, you can expect to receive one of the two pain management methods during your surgery and then be monitored for how well it works in reducing pain afterward. The trial aims to improve pain control for patients undergoing these types of surgeries and ensure their recovery is as comfortable as possible.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • patients Age from 21 to 60 years ,Male and female patients ,ASA I, II patients scheduled for elective abdominoplastic surgeries during the study duration.
  • Exclusion Criteria:
  • Patient refusal, Age less than 21 and above 60 years old, ASA III, IV patients., Infection at the site of injection, Opioid addiction, Allergy to any used substances (lidocaine, bupivacaine)., Preexisting severe or uncontrolled respiratory, renal or cardiac disease. , INR more than 1.5 and platelets less than 100000.

About Cairo University

Cairo University, a premier institution in Egypt, is dedicated to advancing medical research and education through innovative clinical trials. With a strong emphasis on improving healthcare outcomes, the university collaborates with various stakeholders to conduct rigorous scientific studies that address critical health challenges. Leveraging its extensive resources and expert faculty, Cairo University aims to contribute valuable insights to the medical community and enhance patient care both locally and globally. Through its commitment to ethical research practices and excellence, the university plays a pivotal role in shaping the future of healthcare in the region.

Locations

Cairo, , Egypt

Patients applied

0 patients applied

Trial Officials

Hassan Mohamed Ali, Phd

Study Director

Professor of anesthesia Cairo university faculty of medicine

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported