Ultrasound-Guided External Oblique Intercostal Plane Block Versus Subcostal Transversus Abdominis Plane Block For Perioperative Analgesia in Laparoscopic Sleeve Gastrectomy

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-65
SponsorBenha University

About this trial

This study aims to compare the analgesic efficacy, duration of analgesia, and overall opioid consumption between the external oblique intercostal plane (EOIP) block and subcostal transversus abdominis plane (TAP) block in patients undergoing laparoscopic sleeve gastrectomy.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Age from 18 to 65 years.

Both genders.

American Society of Anesthesiologists (ASA) class I or II

Body mass index (BMI) between 30-50 kg/m².

Disqualifiers

Patient refusal.

Allergy to local anesthetics.

Coagulation disorders or anticoagulant therapy.

Local infection or scar at the injection site.

Trial design

Design model

Parallel

Treatments tested in this trial

  • External oblique intercostal plane block

    Other intervention

    Patients will receive an ultrasound-guided bilateral external oblique intercostal plane (EOIP) block using 20 mL of 0.25% bupivacaine in each side after induction of anesthesia and prior to surgical incision.

  • Subcostal transversus abdominis plane block

    Other intervention

    Patients will receive a bilateral subcostal transversus abdominis plane (TAP) block using 20 mL of 0.25% bupivacaine in each side, under ultrasound guidance and identical conditions.

Treatment groups

70 Participants
are divided into 2 treatment groups
Group A: EOIP Group (Group A )Experimental treatment 1 intervention
Group B: Subcostal TAP Group (Group T)Experimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Total morphine consumption

Patient-controlled analgesia (PCA) using intravenous morphine (1 mg bolus, 10-minute lockout) will be available for rescue analgesia when visual analogue score ( VAS ) \> 3.

Time frame
24 hours postoperatively

Secondary outcomes

1

Time to first rescue analgesia

Time to first rescue analgesia will be recorded from the end of surgery till first dose of morphine administrated.

Time frame
24 hours postoperatively
2

Degree of pain

Each patient will be instructed about postoperative pain assessment with the visual analogue score (VAS). VAS (0 represents "no pain" while 10 represents "the worst pain imaginable"). VAS will be recorded at 0, 2, 6, 12, and 24 hours postoperatively (at rest and cough).

Time frame
24 hours postoperatively
3

Heart rate

Heart rate will be recorded intraoperatively and postoperatively

Time frame
Till the end of surgery (Up to two hours)
4

Mean arterial blood pressure

Mean arterial blood pressure will be recorded intraoperatively and postoperatively

Time frame
Till the end of surgery (Up to two hours)

Other outcomes

Sponsors and contacts

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