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Bilateral External Oblique Intercostal Plane Block in Post Operative Pain Management in Hepatectomy

Bilateral External Oblique Intercostal Plane Block Versus Patient Controlled Analgesia (PCA) in Post Operative Pain Management in Hepatectomy Surgery.

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06822309
Acronym
EOI
Enrollment
40
Registered
2025-02-12
Start date
2025-04-01
Completion date
2025-11-01
Last updated
2025-02-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Provide Post Hepatectomy Pain Control

Keywords

External Oblique Intercostal block, subcostal incision, hepatectomy, Patient control analgesia

Brief summary

The majority of cases undergoing hepatectomy suffer from inadequate postoperative analgesia. Therefore, multimodal analgesic techniques are required to relieve pain and discomfort such as intravenous, and epidural analgesia, and peripheral nerve blocks. Although epidural catheters are efficient to provide perioperative analgesia, in this type of surgery patients may be more susceptible to catheter related complications due to the alteration in coagulation parameters. That is why safer alternatives are sought for those patients. The use of patient-controlled analgesia (PCA) for postoperative pain management improves patients' quality of recovery. However, there are many concerns regarding the type of opioids used in PCA such as overdosing, underdosing, and the effect of the hepatectomy on the drug metabolism in those patients. External oblique intercostal plane block (EOI block) is a relatively novel block used in upper abdominal incisions especially subcostal laparotomy to provide intraoperative and postoperative analgesia. This study aims to compare the efficacy of Bilateral External Oblique Intercostal Plain Block versus PCA in pain management and reduction of opioid use in hepatectomy surgery done by subcostal incision.

Interventions

PROCEDUREExternal Oblique Intercostal Plane Block

The block is performed before skin incision by a specialized anesthetist. With the patient positioned in the supine position with their ipsilateral arm abducted, the skin was sterilized, using the high frequency linear probe (M-Turbo HF 38 transducer 13- 6 MHz) of Fujifilm Sonosite ultrasound is placed over the sixth rib medial to the anterior axillary line approximately in midclavicular line in a parasagittal orientation. A 20-guage needle is inserted in a cephalocaudal direction, and the external oblique intercostal plane was hydro dissected with saline. After hydro dissection, the needle is advanced 1 to 2 cm, and 20 mL of 0.25% bupivacaine (Sunny Pharmaceutical) with 4 mg dexamethasone as an additive was administered. The same procedure will be done at the other side (bilateral external oblique intercostal plane block).

DEVICEPatient controlled analgesia

Patients in group will receive intravenous patient controlled analgesia device 100 ml (Accuafuser 100 mL, basal rate 4 mL/hr., bolus 0.5 mL/time, and lock time 15 minutes) for postoperative pain management that will contain 30 mg morphine (loading dose0.1mg/kg) will be given by infusion over 10 minutes then accuafuser will be connected),8 mg dexamethasone and 8 mg ondansetron diluted in 100 ml saline.

Sponsors

Sherif Alaa Embaby
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Age ≥ 18 and ≤ 65 Years. * Both sexes. * Patients will be scheduled for hepatectomy surgery. * Body mass index (BMI) 18.5-30.0 /m 2 .

Exclusion criteria

* Extension of the surgical incision beyond coverage of T12 dermatome. * Prolonged time of surgery > 5 hours. * Hepatectomy surgery combined with another organ resection. * Patients with hypersensitivity to local anesthetics. * History of psychiatric problems. * Recent history of analgesic drugs including opioid abuse or addiction. * Coagulopathy (International normalized ratio \[INR\] > 1.4). * Localized infection at the block site. * Morbidly obese patients.

Design outcomes

Primary

MeasureTime frame
• Rescue morphine consumption in both groups. (Total consumption of morphine rescue shots in milligram in first 2r hours)twenty four hours.

Contacts

Primary ContactSherif A Embaby, Consultant
sherif.embaby@kasralainy.edu.eg+447777918923

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026