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NCT07061678

The Effect of Dexamethasone Administration Route in Pediatric Brachial Plexus Block

Recruiting now Phase 4 Last updated 25 November 2025
What this trial tests

Phase 4 trial testing perineural dexamethasone in Arm in 90 participants. Currently enrolling.

Timeline
1 October 2025
Primary endpoint
30 December 2025
28 February 2026

Quick facts

Lead sponsorPoznan University of Medical Sciences
PhasePhase 4
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingquadruple
Primary purposetreatment
Enrollment90
Start date1 October 2025
Primary completion30 December 2025
Estimated completion28 February 2026
Sites2 locations across Poland

Drugs / interventions tested

Conditions studied

Sponsor

Poznan University of Medical Sciences

Who can join

Adults 3 Months to 6, any sex, with Arm. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other Poznan University of Medical Sciences trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT07061678.

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