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.

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age21-60
SponsorCairo University

About this trial

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.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

patients Age from 21 to 60 years ,Male and female patients ,ASA I, II patients scheduled for elective abdominoplastic surgeries during the study duration.

Disqualifiers

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

Design model

Crossover

Treatments tested in this trial

  • Erector spinae plane block

    Procedure/Surgery

    the patient will recieve ultrasound guided erector spinae plane blockbe. A 20-gauge needle will be placed between the erector spinae muscle and the thoracic transverse processes at the level of T10 using an 'in plane' technique, 20 ml of (0.25% bupivacaine and 1% xylocaine) will be injected on each side.

  • Rectus sheath block

    Procedure/Surgery

    the patient will recieve ultrasound guided rectus sheath block. An 18-gauge needle will be introduced- in plane- just below the costal margin at an angle of approximately 45 degrees to the skin between the rectus abdominis muscle and posterior rectus sheath. 10 ml of (0.25% bupivacaine and 1% xylocaine) will be injected on each side.

Treatment groups

40 Participants
are divided into 2 treatment groups
Group A: Group AActive comparator 2 interventions
Group B: Group BActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Primary outcome

Visual Analogue Scale (VAS) measures pain intenesity one hour after extubation

Time frame
one hour

Secondary outcomes

1

Secondary Outcome

Total morphine consumption during 1st 24 hours postoperatively

Time frame
first 24 hours postoperative
2

Secondary Outcome

Total intraoperative fentanyl consumption.

Time frame
During opration

Other outcomes

Sponsors and contacts

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