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Enrolling by invitation Not applicable

Comparing Postoperative Analgesic Techniques for Umbilical Hernia Repair: A Randomized Trial of Ultrasound Guided Caudal, Erector Spinae, and External Oblique Interfascial Plane Blocks

NCT06948253 · tracked via the Priya Life Science Egypt tracker
Phase
Not applicable
Started
2025-04-10
Last updated
2025-04-29

Condition(s) studied

Regional Anesthesia

Investigational drug(s) / intervention(s)

Erector Spinae Plane BlockCaudal Block AnesthesiaExternal Oblique Intercostal Plane Block

Erector Spinae Plane Block: The correct location of the needle tip in the fascial plane deep to the erector spinae muscle will be confirmed by injecting 0.5-1 ml of saline and observing the fluid lifting the erector spinae muscle off the transverse process while avoiding muscle distension (hydro dissection)

Caudal Block Anesthesia: The needle will be advanced at a 20-degree angle with needle tip and length visualization. A pop can be appreciated as the needle passes through the sacrococcygeal ligament. Once the needle will be confirmed to be in the caudal space on the screen, carefully aspirate to confirm absence of CSF or blood.

External Oblique Intercostal Plane Block: the needle will be advanced until the tip lay in the plane between the external oblique muscle and intercostal muscles between the sixth and seventh ribs

Study summary

The aim of this study is to evaluate the efficacy of ultrasound guided Erector block versus caudal block versus external oblique intercostal plane block perioperatively

Eligibility

Sex
ALL
Min age
2 Years
Max age
7 Years
Healthy volunteers
Accepted
Inclusion Criteria: * pediatric patients of both sexes undergoing elective umblical hernia surgeries aged from 2 year to 7 years belonging to ASA I or II. Exclusion Criteria: * Parents refusal. * Coagulopathy. * Allergy to local anesthesia. * Local infection at the site of injection. * Neurological anomalies.

Primary outcome measure(s)

  • Primary outcome — 15 minute after operation , 30 minutes after operation and 4 h after operation
    Faces Legs Activity Cry Consolability tool (FLACC, 0- 10)

Trial sites (1)

FacilityCityRegionStatus
Mohamed Zakarea Wfa Tanta Egypt
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 NCT06948253 on ClinicalTrials.gov ↗ ← All trials in Egypt