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NCT07056946Completed

Supra Inguinal Fascia Iliaca Block Versus Ultrasound-guided Caudal Analgesia for Pediatrics Undergoing Anterior and Lateral Thigh Surgeries: A Randomized Controlled Trial

Source: ClinicalTrials.gov · Last updated 15 Sept 2026

Brief summary (registry, in English)

patients will then be randomized in the two groups. 1. Group C: in this group children will receive US-guided caudal analgesia (CA) after GA. The caudal block will be performed 2. Group B: in this group children will receive lower limb peripheral nerve blocks in the form of US-guided fascia iliaca Block.

Status (registry)
Completed
Study type
Interventional
Enrollment
70 (actual)
First submitted
29 Jun 2025
Start date
Aug 2025
Primary completion date
Aug 2026
Lead sponsor
National Cancer Institute, Egypt
NCT number
NCT07056946

What you commit to

  • Study type: Interventional
  • Participants enrolled: 70
  • From Aug 2025 to the primary completion date, Aug 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Allergy to any local anesthetics

Other

  • Refusal of parental consent

Who the study is looking for

  • Age 1-7 years
  • scheduled for anterior and lateral thigh Surgeries
  • American Society of Anesthesiologists (ASA) physical status II or III

Age in the registry: 1 year to 7 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
National Cancer Institute
Coordinator of this site? Confirm its status
CairoEgyptUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.