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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.

Cairo University (CU) logo

Cairo University (CU)

Status

Enrolling

Conditions

Perioperative Analgesia
Abdominoplasty

Treatments

Procedure: Rectus sheath block
Procedure: Erector spinae plane block

Study type

Interventional

Funder types

Other

Identifiers

NCT06765772
MS-370-2024

Details and patient eligibility

About

The goal of this clinical trail is to determine if bilateral erector spinae plane block alone can provide good perioperative analgesia for abdominoplastic surgery patients or it is better to give combined bilateral rectus sheath and erector spinae plane blocks to achieve effective intraoperative and postoperative analgesia with minimal morphine consumption in such operations in which there is an extensive surgical dissection and a high risk of respiratory problems.

Full description

This study is randomized controlled trail in which 40 adult patients (male or female) scheduled for elective abdominoplastic surgeries during the study duration will be randomized into to equal groups to investigate the efficacy of erector spinae plane block alone versus the efficacy of combine use of erector spinae and rectus sheath plane block for intra and postoperative analgesia in abdominoplastic surgery patients.

Enrollment

40 estimated patients

Sex

All

Ages

21 to 60 years old

Volunteers

No Healthy Volunteers

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.

Trial design

Primary purpose

Diagnostic

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Double Blind

40 participants in 2 patient groups

Group A
Active Comparator group
Description:
20 Adult patients scheduled for elective abdominoplastic surgeries under general anethesia
Treatment:
Procedure: Erector spinae plane block
Procedure: Rectus sheath block
Group B
Active Comparator group
Description:
20 Adult patients scheduled for elective abdominoplastic surgeries under general anethesia
Treatment:
Procedure: Erector spinae plane block

Trial contacts and locations

1

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Central trial contact

yahya Mohamed Hammad, MD

Data sourced from clinicaltrials.gov

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