Skip to main content
OpenTrials
Completed

NCT Number: NCT07055438

Bilateral External Oblique Intercostal Plane Bock (EOIPB) in Upper Abdominal Surgeries

The current study is designed to investigate the analgesic potentials of two modalities of abdominal blocks where local anesthetics is injected in the fascial planes of the abdominal muscles to anesthetize the nerves supplying the abdomen in patients undergoing upper abdomial surgeries.

the two modalities are the rectus sheath block (RSB) and the external oblique intercostal plane block (EOIPB). The investigators are going to use the ultrasound to identify the muscles and inject the local anesthetics. The investigators suggest that the EOIPB might provide better pain control when compared to RSB.

Completed

Looking for future studies?

Notify Me

Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Kasr El Ainy, Cairo, Egypt

Loading trial locations.

About this study

Fascial plane blocks emerge as an appealing technique to provide good intraoperative and postoperative analgesia in patients undergoing upper abdominal surgeries. Such techniques have the benefit of decreasing opioids use and consequently reducing the like hood of their side effects.

Ultrasound guided rectus sheath Block (RSB) targets the terminal branches of thoracic nerves thus providing analgesia for midline abdominal incisions.

Ultrasound guided external oblique intercostal plane block (EOIPB), a relatively new technique, targets the lateral cutaneous branches of the thoracoabdominal nerves providing analgesia for anterolateral and upper median plane of the abdomen.

Studies Comparing both techniques are deficient, that is why the investigators designed the current study to evaluate and compare the analgesic efficacy of both techniques in upper abdominal surgeries namely Whipple operation and total gastrectomy.

The study is a randomized controlled double blinded trial comprising two groups. The RSB group will receive bilateral ultrasound guided rectus sheath block with 20ml of 0.25% bupivacaine on each side. The EOIB group will receive bilateral ultrasound guided External oblique intercostal plane block with 20ml of 0.25% bupivacaine on each side as well. Both blocks will be performed after administering general anesthesia.

The main endpoint of the study is the time to first request for rescue analgesia.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Age from 18 to 65 Years
  • Both sexes.
  • American Society of Anesthesiologists (ASA) physical status II, III.
  • Patients who will undergo upper abdominal surgeries (Whipple operation, total gastrectomy).

Exclusion criteria

  • Coagulation disorders.
  • Abdominal surgery history.
  • Infection in the block application area.
  • Chronic opioid use.
  • Local anesthetic (LA) allergy.
  • Pregnancy.
  • BMI ≥35 kg/m2.
  • Severe cardiovascular problems.
  • Diabetic neuropathy.
  • Complicated surgeries with massive blood loss and hemodynamic instability.

Treatment and study plan

Ultrasound guided Rectus sheath block

Procedure

After receiving general anesthesia, bilateral ultrasound guided rectus sheath block with 20 ml of 0.25% bupivacaine on each side will be administered to 20 patients undergoing upper abdominal surgeries namely whipple operation and total gastrectomy

ultrasound guided external oblique intercostal plane block

Procedure

After receiving general anesthesia, bilateral ultrasound guided external oblique intercostal plane block with 20 ml of 0.25% bupivacaine on each side will be administered to 20 patients undergoing upper abdominal surgeries namely whipple operation and total gastrectomy

Primary outcomes

  1. Time to first request for rescue analgesia

    Time frame: Time in hours from end of surgery to first dose of morphine administered up to 24 hours postoperatively

    Time from end of surgery to first dose of morphine administered

Secondary outcomes

  1. Fentanyl consumption

    Time frame: From the start of the surgery till the end in micogram/Kg

    Intraoperative fentanyl consumption

  2. Postoperative morphine consumption

    Time frame: from the time numerical rating scale exceeds 3 and till 24 hours after the end of the surgery

    Total morphine consumption (mg) in the first 24hrs after surgery

  3. Pain score

    Time frame: from the time of recovery immediately in the postoperative period and then at 30 minutes, 1 hour, 2 hours, 4 hours, 6 hours, 12 hours and 24 hours postoperatively

    Pain score using Numerical rating Scale (NRS)between 0 and 10, Zero means no pain and ten means the worst pain

  4. Patient satisfaction of analgesia

    Time frame: 2 hours after recovery from anesthesia

    Degree of patient satisfaction will be assessed on a 5-point Likert scale patient satisfaction (1, extremely dissatisfied; 2, unsatisfied; 3, neutral; 4, satisfied ; 5, extremely satisfied)

  5. Incidence of postoperative nausea and vomiting

    Time frame: From the recovery of anesthesia and up to 24 hours postoperatively

    The number of patients suffering from postoperative nausea and vomiting in both groups

Sponsors and collaborators

Lead sponsor

Kasr El Aini Hospital

Other

Registry information

Official study title

Analgesic Efficacy of Ultrasound Guided Bilateral External Oblique Intercostal Plane Block Versus Rectus Sheath Block in Upper Abdominal Surgeries: A Randomized Double-blinded Controlled Study

Important dates

Study start
2025
Primary completion
2025
Study completion
2025
First posted
Jul 8, 2025
Registry last updated
Dec 2, 2025

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.

Published trials that share one or more normalized conditions with this study.