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NCT07411274Not yet recruitingPhase 3

Ultrasound-Guided vs. Conventional Scalp Block for Postoperative Analgesia in Pediatric Supratentorial Tumor Surgeries

Comparison of Ultrasound-Guided vs. Conventional Scalp Block for Postoperative Analgesia in Pediatric Supratentorial Tumor Surgeries: A Randomized Controlled Trial.

Source: ClinicalTrials.gov · Last updated 13 Feb 2026

Brief summary (registry, in English)

Although scalp nerve blocks have been shown to provide effective postoperative analgesia in pediatric neurosurgical procedures, limited data exist on their use under ultrasound guidance. The smaller anatomical structures and higher vascularity of the pediatric scalp increase the risk of inadvertent vessel puncture or systemic toxicity with landmark-based techniques. Ultrasound guidance enables direct visualization of the targeted nerves and adjacent vessels, potentially improving block accuracy and safety. To date, no randomized controlled trial has compared ultrasound-guided versus conventional scalp block specifically in pediatric supratentorial tumor surgeries. This study aims to fill this gap.

Status (registry)
Not yet recruiting
Phase (registry)
Phase 3
Study type
Interventional
Enrollment
74 (estimated)
First submitted
26 Jan 2026
Start date
Feb 2026
Primary completion date
Oct 2026
Lead sponsor
Cairo University
NCT number
NCT07411274

What you commit to

  • Study type: Interventional · Phase 3
  • Planned participants: 74
  • From Feb 2026 to the primary completion date, Oct 2026
  • No sites listed in no 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 local anesthetics.
  • Pre-existing bradycardia (HR \<60 bpm in infants, \<50 bpm in older children) or unstable arrhythmias.
  • Severe hepatic/renal impairment.

Lab values

  • Coagulopathy or platelet dysfunction.

Other

  • Urgent/emergency craniotomy.

Who the study is looking for

  • American Society of Anesthesiologists (ASA) physical status I, II.
  • Undergoing elective supratentorial tumor surgery under general anesthesia on one side of the head.

Age in the registry: 2 years to 12 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

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