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US Guided EOI Block Versus ESPB for Postoperative Analgesia in Laparoscopic Cholecystectomy

A

Assiut University

Status

Enrolling

Conditions

Postoperative Pain

Treatments

Other: External oblique intercostal (EOI) block
Other: Erector spinae plane block (ESPB)

Study type

Interventional

Funder types

Other

Identifiers

NCT05272280
ABC-5-DE

Details and patient eligibility

About

To compare the efficacy of USG-guided bilateral External oblique intercostal (EOI) block with Erector spinae plane block (ESPB) for post-operative analgesia after laparoscopic cholecystectomy with a hypothesis that both External oblique intercostal fascial plane block and Erector spinae plane block are effective in providing post-operative analgesia.

Enrollment

50 estimated patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age between 18 and 65 years with a body mass index (BMI) of 18-35 kg/m2,
  • patients with the American Society of Anesthesiologists (ASA) physical status I/II,
  • Patients scheduled for elective laparoscopic cholecystectomy.

Exclusion criteria

  • Allergy to local anaesthetics,
  • Infection at the site of injection,
  • Coagulopathy,
  • Chronic pain syndromes,
  • Prolonged opioid medication,
  • Patients who received any analgesic 24 h before surgery.

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

50 participants in 2 patient groups

External oblique intercostal (EOI) block
Active Comparator group
Treatment:
Other: External oblique intercostal (EOI) block
Erector spinae plane block (ESPB)
Active Comparator group
Treatment:
Other: Erector spinae plane block (ESPB)

Trial contacts and locations

1

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Central trial contact

Amr M.A. Thabet, MD; Magdy M mahdy, MD

Data sourced from clinicaltrials.gov

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