About this trial

The purpose of this study is to understand the trajectory of function and self-reported outcomes of patients following pelvic and acetabular, treated both operatively and nonoperatively.

Eligibility criteria

Qualifiers

Fracture of the pelvic ring

Fracture of the acetabulum

Disqualifiers

Patients unwilling to provide consent to participate.

Trial design

Treatments tested in this trial

  • Operative
  • Nonoperative

Treatment groups

200 Participants
are divided into 2 treatment groups

Locations

1
Atrium Health- Carolinas Medical Center28203, CharlotteNorth Carolina, United States

Sponsors and collaborators

Wake Forest University Health Sciences

Lead sponsor