Comparing Dexmedetomidine and Dexamethasone for Pain Relief in Children After Ankle Surgery
Perineural Dexmedetomidine Vs Dexamethasone on the Duration of Popliteal Nerve Block for Anesthesia After Pediatric Ankle Surgery
This study is testing whether adding Dexmedetomidine or Dexamethasone to pain relief shots can help kids feel less pain and recover faster after ankle surgery.
Quick facts
| Phase | Phase 4 |
|---|---|
| Study type | Interventional |
| Enrollment | 90 (estimated) |
| Ages | 3 Months to 18 Years |
| Sex | All |
| Sponsor | Poznan University of Medical Sciences Academic / other |
| Locations | 1 site (Poznań, Wielkopolska) |
| Trial ID | NCT06304324 on ClinicalTrials.gov |
What this trial studies
This study investigates the effectiveness of perineural Dexmedetomidine versus Dexamethasone in prolonging the duration of popliteal nerve blocks for pain management following pediatric ankle and foot surgeries. The research aims to determine which adjuvant provides better analgesia and faster recovery for children undergoing these procedures. By comparing two different medications added to local anesthetics, the study seeks to enhance postoperative pain control while ensuring safety in a pediatric population. The trial is conducted at the Poznan University of Medical Sciences in Poland.
Who should consider this trial
Good fit: Ideal candidates for this study are children scheduled for foot or ankle surgery who weigh more than 5 kg.
Not a fit: Patients with infections at the site of the nerve block, coagulation disorders, or those on regular steroid medication may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved pain management strategies for children undergoing ankle and foot surgeries.
How similar studies have performed: While there is considerable research on dexamethasone use in adults, this study is novel as it focuses specifically on pediatric patients.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * children scheduled for foot/ankle surgery * body weight \> 5kg Exclusion Criteria: * infection at the site of the regional blockade * coagulation disorders * immunodeficiency * ASA= or \>4 * steroid medication in regular use
Where this trial is running
Poznań, Wielkopolska
- Department of Spine Diseases and Pediatric Orthopedics, University of Medical Sciences, Poznań, Poland — Poznań, Wielkopolska, Poland (Recruiting)
Study contacts
- Study coordinator: Malgorzata Domagalska, PhD
- Email: m.domagalska@icloud.com
- Phone: 608762068
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.