Clinical Trial

The Effect of Dexamethasone Administration Route in Pediatric Brachial Plexus Block

Completed Phase 4
View on ClinicalTrials.gov →
Summary
This study aims to assess the impact of the administration route of dexamethasone (intravenous vs. perineural) on postoperative pain and inflammatory response in pediatric patients undergoing hip surgery. The primary outcome is postoperative pain intensity measured using an age-appropriate scale at multiple intervals. Secondary outcomes include inflammatory markers such as neutrophil-to-lymphocyte ratio (NLR) and platelet-to-lymphocyte ratio (PLR), opioid consumption, time-to-first rescue analgesia, and overall patient recovery. This randomized, double-blinded study seeks to improve pain management strategies and optimize anesthesia protocols in pediatric arm surgery.
Protocol Amendment History 1 change
critical Trial completed 2026-07-31
Trial Details
NCT Number NCT07061678
Lead Sponsor Poznan University of Medical Sciences
Conditions Arm
Enrollment 90 participants
Start Date 2025-10-01
Primary Completion 2026-05-30 (estimated)
Study Completion 2026-06-15 (estimated)
Updated on ClinicalTrials.gov 2026-07-30