Comparing two pain relief methods for patients undergoing abdominoplasty

Is this trial a fit for you?

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

What this trial studies

This clinical trial aims to evaluate the effectiveness of a combined approach using bilateral rectus sheath and erector spinae plane blocks versus using the erector spinae plane block alone for pain management in patients undergoing elective abdominoplastic surgeries. The study will involve 40 adult patients who will be randomly assigned to one of the two groups to assess their pain relief outcomes and morphine consumption during and after surgery. The goal is to determine which method provides better analgesia with fewer side effects, particularly in patients at risk for respiratory complications.

Why it matters

Who can join: the full rules

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.

Where it's running

• Cairo university hospital
  Cairo, Cairo Governorate, Egypt Recruiting

Study contacts

• Study coordinator: yahya Mohamed Hammad, MD
• Email: yahya196cm@hotmail.com
• Phone: 00201114048081

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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.