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Clinical Trials in Egypt / NCT07624058
Recruiting Not applicable

Erector Spina Plane Block Versus Modified Thoracoabdominal Nerve Block After Laparoscopic Cholecystectomy

NCT07624058 · tracked via the Priya Life Science Egypt tracker
Phase
Not applicable
Started
2026-04-01
Last updated
2026-06-03

Condition(s) studied

Erector Spinae BlockModified Thoracoabdominal Nerve BlockLaparoscopic Cholecystectomy

Investigational drug(s) / intervention(s)

bilateral ESP blockbilateral M-TAPA block

bilateral ESP block: bilateral ESP block with injection of 20 ml 0.25% bupivacaine.

bilateral M-TAPA block: bilateral M-TAPA block with injection of 20 ml of 0.25% bupivacaine.

Study summary

direct comparisons between ESPB and M-TAPA for postoperative analgesia after LC remain limited. This is an important area of clinical interest because the two blocks differ significantly in their anatomical targets, mechanism of analgesia, and likely dermatomal coverage. The ESPB provides analgesia through paravertebral spread affecting both dorsal and ventral rami, thereby offering posterior and visceral pain relief, whereas M-TAPA directly targets the thoracoabdominal nerves, resulting in better anterior and lateral abdominal wall analgesia. Understanding which technique offers superior or more balanced analgesia could help to optimise regional anaesthesia strategies in LC and to improve patient outcomes.

Eligibility

Sex
ALL
Min age
30 Years
Max age
65 Years
Healthy volunteers
No
Inclusion Criteria: * Age: between 30 - 65 * American Society of Anaesthesiologists physical status: I- III * Body mass index: 18-35 kg.m-2 Exclusion Criteria: * Patient Refusal * Allergy to local anaesthetic agents. * Skin infection at the site of injection. * Coagulopathy. * Diabetes Mellitus

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Alexandria University Alexandria Egypt Recruiting

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07624058 on ClinicalTrials.gov ↗ ← All trials in Egypt