The Effect of Dexamethasone Administration Route in Pediatric Brachial Plexus Block

ConditionArm
Trial statusRecruiting
Trial phasePhase 4
Trial typeInterventional
Biological sexAll
Age3-6
SponsorPoznan University of Medical Sciences

About this trial

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.

Eligibility criteria

Qualifiers

children scheduled for arm/wrist/hand surgery

body weight > 5kg

Disqualifiers

infection at the site of the regional block,

coagulation disorders,

immunodeficiency,

American Society of Anesthesiologists (ASA) physical status of IV or higher,

Trial design

Treatments tested in this trial

  • perineural dexamethasone
  • intravenous dexamethasone
  • 0.2ml/kg 0.2% ropivacaine

Treatment groups

90 Participants
are divided into 3 treatment groups