External Oblique Intercostal Block Versus Erector Spinae Plane Block on Postoperative Pain in Laparoscopic Radical Gastrectomy

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorGeneral Hospital of Ningxia Medical University

About this trial

Postoperative pain is highly prevalent following laparoscopic radical gastrectomy. Although the erector spinae plane block (ESPB) can effectively alleviate this pain, it still has many limitations. The external oblique intercostal plane block (EOIB) is a novel nerve block technique that may provide well postoperative analgesia for upper abdominal surgery. Therefore, this study employs a non-inferiority randomized controlled trial design to verify that the analgesic effect of EOIB is not inferior to that of ESPB, thereby offering more options for regional analgesia strategies in laparoscopic radical gastrectomy.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Patients aged over 18 years

Classified as ASA I-III

Scheduled for elective laparoscopic radical gastrectomy under general anesthesia

Voluntarily participated and provided written informed consent.

Disqualifiers

Chronic opioid dependence or prior use of analgesic medications for >3 months;

Inability to communicate due to severe dementia, language barriers, or terminal illness;

History of central and/or peripheral nervous system disorders;

Severe renal insufficiency (serum creatinine >442 μmol/L or requiring renal replacement therapy) or severe hepatic insufficiency (Child-Pugh class C);

Trial design

Design model

Parallel

Treatments tested in this trial

  • External Oblique Intercostal Plane Block

    Procedure/Surgery

    With the patient in the supine position, a high-frequency linear array probe (6-15 MHz) is used to perform a sagittal parasagittal oblique scan at the level of the 6th rib, between the right anterior axillary line and midclavicular line. The external oblique muscle, intercostal muscles, and ribs are identified. Using an in-plane technique, a 21G, 100mm block needle is inserted from a superomedial to inferolateral direction, with the needle tip positioned in the plane between the external oblique muscle and the intercostal muscles at the caudal edge of the 6th rib. 30ml of 0.375% ropivacaine is injected on each side, for a bilateral administration.

  • Erector Spinae Plane Block (ESPB) group

    Procedure/Surgery

    With the patient in the lateral decubitus position (surgical side up), a low-frequency convex array probe (2-5 MHz) is used to perform a sagittal scan approximately 2-3 cm lateral to the spinous process of T8 or T9. The transverse process and the erector spinae muscle are identified. Using an out-of-plane technique, a 21G, 100mm block needle is advanced until contact is made with the transverse process. The needle is then withdrawn 1-2 mm to position its tip within the fascial plane deep to the erector spinae muscle and superficial to the transverse process. 30 ml of 0.375% ropivacaine is injected on each side, for a bilateral administration.

Treatment groups

184 Participants
are divided into 2 treatment groups
Group A: ESPBExperimental treatment 1 intervention
Group B: EOIBExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Cumulative opioid consumption within 24 hours postoperatively

Cumulative opioid consumption within 24 hours postoperatively. Conversion to morphine equivalent dose (mg)

Time frame
24 hours after surgery

Secondary outcomes

1

Pain Intensity

Pain at rest and during coughing will be assessed using the Numerical Rating Scale (NRS, 0-10) at 2, 6, 12, 24, 48, and 72 hours postoperatively.0 represents no pain, and 10 represents the most pain.

Time frame
2, 6, 12, 24, 48, and 72 hours postoperatively
2

Quality of Recovery

The 15-item Quality of Recovery scale (QoR-15) was used for assessment at 24, 48, and 72 hours postoperatively. The higher the score, the better the recovery quality

Time frame
24,48,72 hours after surgery
3

sleep quality

Sleep quality was assessed using the Richards-Campbell Sleep Questionnaire (RCSQ) on postoperative nights.0 points represent very poor sleep, while 100 points represent very good sleep

Time frame
24,48,72 hours after surgery

Other outcomes

Sponsors and contacts

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