Actively Recruiting

Age: 18Years +
All Genders
ID04615104

Functional, Clinical, and Performance Outcomes Following Pelvic and Acetabular Fracture: A Prospective Observational Study

Led by Wake Forest University Health Sciences · Updated on 2025-11-21

200

Participants Needed

1

Research Sites

104 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This research aims to understand how patients recover in terms of function and self-reported outcomes after experiencing pelvic or acetabular fractures. It includes patients treated with surgery or without surgery and seeks to answer important questions about these treatments by capturing data over time. Patients in the study are grouped based on having either pelvic ring fractures or acetabular fractures. The study collects information regardless of whether the treatment was operative (surgical) or nonoperative (nonsurgical). Various performance and patient-reported outcome measures, including the NIH PROMIS tool, are used to monitor recovery. Participants will be followed for up to 24 months after their injury. During this time, researchers will assess their return to work and daily activities, track fracture healing and complications, and evaluate physical performance through tests like the 10 meter walk, Five Time Sit to Stand, and Timed Up and Go. Patient feedback is collected at multiple time points to understand their health status and function over time.

CONDITIONS

Brief Title

Pelvic and Acetabular Fracture: A Prospective Observational Study

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Fracture of the pelvic ring
  • Fracture of the acetabulum
  • Age 18 years or older
  • Willingness to provide consent to participate
Not Eligible

You will not qualify if you...

  • Patients unwilling to provide consent to participate

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Monitoring

Duration - Up to 24 months following injury

Participants who have sustained pelvic or acetabular fractures are observed to collect data on functional and self-reported outcomes over time, regardless of treatment type.

Assessments at baseline, 3, 6, 12, and 24 months

Trial Site Locations

Total: 1 location

1

Atrium Health- Carolinas Medical Center

Charlotte, North Carolina, United States, 28203

Actively Recruiting

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Research Team

C

Christine Churchill, MA

E

Erica Grochowski, MS

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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Frequently Asked Questions

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Published Research Related To This Trial

Pelvic fractures: epidemiology and predictors of associated abdominal injuries and outcomes.

Demetrios Demetriades, Marios Karaiskakis, Konstantinos Toutouzas...

https://pubmed.ncbi.nlm.nih.gov/12113532