Comparing two anesthesia techniques for hip fractures in emergency patients
Comparison of Pericapsular Nerve Group Block (PENG) Versus Fascia Iliaca Compartment Block (FICB) for Hip Fracture Analgesia in Emergency Department Patients
This study is testing which of two anesthesia techniques works better to manage pain and reduce weakness in older patients with hip fractures who come to the emergency room.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 50 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | University of Virginia Academic / other |
| Locations | 1 site (Charlottesville, Virginia) |
| Trial ID | NCT05505604 on ClinicalTrials.gov |
What this trial studies
This study evaluates the effectiveness of two regional anesthesia techniques, the Pericapsular Nerve Group (PENG) block and the Fascia Iliaca Compartment Block (FICB), for managing pain in elderly patients with hip fractures presenting to the emergency department. The research aims to determine if the PENG block provides superior pain control and results in less motor weakness compared to the FICB. By measuring pain levels, opioid usage, and motor function, the study seeks to improve pain management strategies for this vulnerable population.
Who should consider this trial
Good fit: Ideal candidates are elderly patients presenting with proximal femur fractures in the emergency department.
Not a fit: Patients with hemodynamic instability or severe medical conditions may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved pain management and reduced opioid use for elderly patients with hip fractures.
How similar studies have performed: Previous studies have suggested that the PENG block may be superior to the FICB, indicating potential success for this approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Proximal femur fracture Exclusion Criteria: * refusal to consent * hemodynamic instability * allergy to local anesthetics * severe injury with instability * severe medical conditions with instability
Where this trial is running
Charlottesville, Virginia
- University of Virginia Medical Center — Charlottesville, Virginia, United States (Recruiting)
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.