Pelvic fractures: epidemiology and predictors of associated abdominal injuries and outcomes.
Demetrios Demetriades, Marios Karaiskakis, Konstantinos Toutouzas...
https://pubmed.ncbi.nlm.nih.gov/12113532Actively Recruiting
Led by Wake Forest University Health Sciences · Updated on 2025-11-21
200
Participants Needed
1
Research Sites
104 weeks
Total Duration
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
Pelvic and Acetabular Fracture: A Prospective Observational Study
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Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
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
Total: 1 location
1
Atrium Health- Carolinas Medical Center
Charlotte, North Carolina, United States, 28203
Actively Recruiting
C
Christine Churchill, MA
E
Erica Grochowski, MS
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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