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Recruiting NCT05272280

NCT05272280 US Guided EOI Block Versus ESPB for Postoperative Analgesia in Laparoscopic Cholecystectomy

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Clinical Trial Summary
NCT ID NCT05272280
Status Recruiting
Phase
Sponsor Assiut University
Condition Postoperative Pain
Study Type INTERVENTIONAL
Enrollment 50 participants
Start Date 2022-05-01
Primary Completion 2025-01

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age 65 Years
Study Type INTERVENTIONAL
Interventions
External oblique intercostal (EOI) blockErector spinae plane block (ESPB)

Eligibility Fast-Check

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What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 50 participants in total. It began in 2022-05-01 with a primary completion date of 2025-01.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

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.

Eligibility Criteria

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.

Contact & Investigator

Central Contact

Magdy M mahdy, MD

✉ magdymahdy84@yahoo.com

📞 0109 650 2058

Frequently Asked Questions

Who can join the NCT05272280 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, up to 65 Years, studying Postoperative Pain. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT05272280 currently recruiting?

Yes, NCT05272280 is actively recruiting participants. Contact the research team at magdymahdy84@yahoo.com for enrollment information.

Where is the NCT05272280 trial being conducted?

This trial is being conducted at Asyut, Egypt.

Who is sponsoring the NCT05272280 clinical trial?

NCT05272280 is sponsored by Assiut University. The trial plans to enroll 50 participants.

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