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Clinical Trials/NCT05505604
NCT05505604
Recruiting
Not Applicable

Comparison of Pericapsular Nerve Group Block (PENG) Versus Fascia Iliaca Compartment Block (FICB) for Hip Fracture Analgesia in Emergency Department Patients

University of Virginia1 site in 1 country50 target enrollmentSeptember 30, 2022

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Femoral Neck Fractures
Sponsor
University of Virginia
Enrollment
50
Locations
1
Primary Endpoint
Pain score
Status
Recruiting
Last Updated
last year

Overview

Brief Summary

Regional anesthesia for hip fractures has been shown to decrease rates of delirium in elderly patients with hip fractures as well as improve pain compared to systemic opioids. The Pericapsular Nerve Group (PENG) block has recently received attention as an alternative approach to femoral nerve block and Fascia Iliaca Compartment Block (FICB). The investigators seek to evaluate if there is a difference between the PENG and FICB in terms of efficacy of pain control in ED patients presenting with hip fracture. We hypothesize that the PENG block may be superior based on previous research.

Detailed Description

Fractures of the proximal femur are a common presentation to the emergency department and are an acutely painful condition. This condition predominantly affects elderly patients who are at risk for delirium and more susceptible to the adverse effects of systemic opioids. Regional anesthesia is an recommended component of pain control for elderly patients with hip fracture. The investigators seek to compare the efficacy of pain control of the Pericapsular Nerve Group (PENG) block with the Fascia Iliaca Compartment Block (FICB). Previous studies have suggested that the PENG block may be superior to the FICB for pain control and results in less thigh motor weakness. The investigators will compare pain control (by difference in mean VAS score at set time points), systemic opioid use (in mean morphine equivalents prior to surgery), and motor function in patients with hip fractures who receive either block in the ED.

Registry
clinicaltrials.gov
Start Date
September 30, 2022
End Date
September 30, 2025
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Matthew Kongkatong, MD

Assistant Professor of Emergency Medicine

University of Virginia

Eligibility 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

Outcomes

Primary Outcomes

Pain score

Time Frame: 6 hours

Median pain score on 0-10 Numeric Rating Scale

Secondary Outcomes

  • Opioid use(From block administration until time of surgery or 24 hours if surgery performed >24 hours)

Study Sites (1)

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