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NCT Number: NCT07617545

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

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.

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Key information

Age range

6 year–12 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Alexandria University

Alexandria, 21526, Egypt

Location status: Recruiting

Location contact

Belal M Hassan, MBBCH

CONTACT

[email protected]

00201091397908

Mohamed W Nassar, MD

SUB_INVESTIGATOR

Ola M Zanaty, MD

SUB_INVESTIGATOR

Wafaa M Shafshak, MD

SUB_INVESTIGATOR

About this study

Paediatric nerve blocks are increasingly recognized as new standard for managing pain in children. The advantages of regional anesthesia in this population include enhanced operating conditions, expedited recovery of bowel function, and reduced postoperative pain.

The caudal epidural block remains the most used method; however, the external oblique intercostal block, a novel technique involves administering local anesthesia deep to the external oblique muscle at the sixth intercostal space, thereby blocking thoracoabdominal nerves from T6 to T10. This technique offers several advantages, including straightforward anatomy, a single muscle strip that is easily identifiable even in obese patients, a bony backstop, and an easily expandable fascial plane that can accommodate a catheter.

The erector spinae plane block involves injecting local anesthetic into the fascial plane beneath the erector spinae muscle at the tip of the vertebral transverse process. This allows the local anesthetic to spread in the craniocaudal fascial plane.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 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.

Exclusion criteria

  • Guardian refusal.
  • Allergy to local anesthetics.
  • Surgical procedures exceeding 3 hours.
  • Infection at the area planned for the block injection.
  • Prolonged opioid medication.
  • Patients preoperatively medicated by Beta blockers

Treatment and study plan

External Oblique Intercostal Plane Block

Other

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

Erector spinae plane block

Other

Patients will receive ultrasound-guided erector spinae plane block.

Primary outcomes

  1. Degree of pain

    Time frame: 12 hours after surgery

    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.

Secondary outcomes

  1. Heart rate

    Time frame: Every 15 minutes intraoperative

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

  2. Mean arterial blood pressure

    Time frame: Every 15 minutes intraoperative

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

  3. Peripheral oxygen saturation

    Time frame: Every 15 minutes intraoperative

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

  4. Duration of analgesia

    Time frame: 12 hours after surgery

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

  5. Total rescue analgesia requirement

    Time frame: 12 hours after surgery

    In Faces Pain Scale score-revised, cut of points for analgesic requirement is ≧ 4, rescue analgesia will be administered in the form of nalbuphine 0.1 mg/kg, with a maximum dose of 0.2 mg/kg.

  6. Incidence of complications

    Time frame: 12 hours after surgery

    Incidence of complications including hematomas block failure, intravascular injection, pneumothorax or injection into the peritoneal cavity, with associated risks of damage to bowel and other abdominal viscera at the block site will be recorded.

Study contacts

Contact information is provided by the study sponsor or research team.

Belal M Hassan, MBBCH

CONTACT

[email protected]

00201091397908

Sponsors and collaborators

Lead sponsor

Alexandria University

Other

Registry information

Official study title

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

Important dates

Study start
2025
Primary completion
2026
Study completion
2026
First posted
Jun 1, 2026
Registry last updated
Jun 1, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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