Geriatric Lateral Compression 1 Pelvic Fractures

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age60-100
SponsorHealthPartners Institute

About this trial

Lateral compression-1 (LC1) pelvic ring fragility fractures cause significant pain and morbidity. These fragility injuries are associated with prolonged immobility and long hospital stays. Currently there is no consensus on operative stabilization of LC1 pelvic fractures, nor are there evidence-based guidelines to aid in management of these injury types. Furthermore, there is variability in operative indications, improvement in pain and mobilization. The purpose of this study is to compare percutaneous screw fixation to non-operative management in symptomatic LC1 fragility fractures in elderly patients.

Eligibility criteria

Qualifiers

Patients >/= 60 years of age

Lateral compression 1 pelvic ring fractures confirmed with plain radiographs, CT and/or MRI

Low energy mechanism of injury or an insufficiency fracture without a precipitating event

Acute injury within four weeks of presentation

Disqualifiers

Dementia

Vertically or rotationally unstable pelvic ring injuries

Pathologic fracture secondary to tumor

Non-ambulatory prior to injury

Trial design

Treatments tested in this trial

  • Percutaneous screw fixation
  • Pain management
  • Physical therapy

Treatment groups

100 Participants
are divided into 2 treatment groups

Sponsors and collaborators

HealthPartners Institute

Lead sponsor

Orthopaedic Trauma Association

Collaborator

Allina Health System

Collaborator