External Oblique Intercostal Plane Block Versus Erector Spinae Plane Block in Paediatric Upper Abdominal Surgeries

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age6-12
SponsorAlexandria University

About this trial

This study aims to compare between ultrasound guided external oblique intercostal plane block and ultrasound guided erector spinae plane block in paediatric upper abdominal surgeries.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Children aged between 6 and 12 years of both sex.

Patients with the American Society of Anesthesiologists (ASA) physical status I/II.

Patients undergoing upper abdominal surgeries involving upper abdominal incisions.

Disqualifiers

Guardian refusal.

Allergy to local anesthetics.

Surgical procedures exceeding 3 hours.

Infection at the area planned for the block injection.

Trial design

Design model

Parallel

Treatments tested in this trial

  • External oblique intercostal plane block

    Other intervention

    Patients will receive ultrasound-guided external oblique intercostal plane block.

  • Erector spinae plane block

    Other intervention

    Patients will receive ultrasound-guided erector spinae plane block.

Treatment groups

40 Participants
are divided into 2 treatment groups
Group A: Group IExperimental treatment 1 intervention
Group B: Group IIExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Degree of pain

Postoperative pain will be assessed using Faces pain score revised. The Faces Pain Scale revised (FPS-R) is a validated self-report instrument designed to measure pain intensity in pediatric populations. The scale comprises a series of facial expressions, ranging from a smiling face at 0, indicating "no pain," to a crying face at 10, indicating "very much pain". Children are instructed to select the face that most accurately reflects their current pain level. The faces are scored (0, 2, 4, 6, 8, 10), providing a quantifiable measure of pain intensity.

Time frame
12 hours after surgery

Secondary outcomes

1

Heart rate

Heart rate will be recorded preoperative basal readings, after induction of anesthesia, during skin incision, and every 15 minutes intraoperative.

Time frame
Every 15 minutes intraoperative
2

Mean arterial blood pressure

Mean arterial blood pressure will be recorded preoperative basal readings, after induction of anesthesia, during skin incision, and every 15 minutes intraoperative.

Time frame
Every 15 minutes intraoperative
3

Peripheral oxygen saturation

Peripheral oxygen saturation will be recorded preoperative basal readings, after induction of anesthesia, during skin incision, and every 15 minutes intraoperative.

Time frame
Every 15 minutes intraoperative
4

Duration of analgesia

Duration of analgesia will be recorded from block completion till first postoperative rescue analgesia requirement.

Time frame
12 hours after surgery

Other outcomes

Sponsors and contacts

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