Using Dexamethasone to Improve Pain Relief After Children's Hand and Wrist Surgery
Effect of Perineural Dexamethasone on the Duration of Supraclavicular Brachial Plexus Block for Anesthesia After Pediatric Hand/Wrist Surgery
This study is testing whether adding Dexamethasone to pain relief after hand and wrist surgery can help children feel less pain and recover faster.
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 (Poznan, Poznań) |
| Trial ID | NCT06086392 on ClinicalTrials.gov |
What this trial studies
This study investigates the effect of perineural Dexamethasone on the duration of supraclavicular brachial plexus block anesthesia in children undergoing hand and wrist surgery. The aim is to determine the optimal dose of Dexamethasone that enhances pain relief while allowing for a lower concentration of local anesthetics. By comparing different doses of Dexamethasone, the study seeks to improve postoperative analgesia and recovery times in pediatric patients. The research addresses a significant gap in knowledge regarding the use of Dexamethasone in children, as most existing studies focus on adults.
Who should consider this trial
Good fit: Ideal candidates for this study are children scheduled for hand or wrist surgery who weigh more than 5 kg.
Not a fit: Patients with infections at the site of the blockade, coagulation disorders, immunodeficiency, or those on regular steroid medication may not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could lead to improved pain management and faster recovery for children after hand and wrist 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, where such research is lacking.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * children scheduled for hand/wrist 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
Poznan, Poznań
- Poznan University of Medical Sciences — Poznan, Poznań, Poland (Recruiting)
Study contacts
- Study coordinator: Malgorzata Domagalska, Ph.D.
- Email: m.domagalska@icloud.com
- Phone: +48 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.