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Effect of Systematic Dexamethasone on the Duration of Popliteal Nerve Block for Anesthesia After Pediatric Ankle Surgery

NCT05887765 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 90

Last updated 2025-09-18

No results posted yet for this study

Summary

Effect of systematic dexamethasone on the duration of popliteal nerve block after pediatric ankle/foot surgery

Conditions

  • Ankle Disease
  • Foot Deformities
  • Foot Diseases
  • Cerebral Palsy

Interventions

DRUG

Sodium Chloride 0.9% Inj

administration of 5ml 0,9% sodium chloride - 30 minutes before the popliteal nerve block

DRUG

0,1mg/kg Dexamethasone

administration of 0,1mg/kg Dexamethasone - 30 minutes before the popliteal nerve block

DRUG

0,2mg/kg Dexamethasone

administration of 0,2mg/kg Dexamethasone - 30 minutes before the popliteal nerve block

Sponsors & Collaborators

  • Poznan University of Medical Sciences

    lead OTHER

Principal Investigators

  • Tomasz Kotwicki, Prof.dr hab. · Poznań University of Medical Sciences

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
3 Months
Max Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2023-10-17
Primary Completion
2025-06-30
Completion
2025-07-29

Countries

  • Poland

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05887765 on ClinicalTrials.gov