Early reduction of acetabular fractures decreases the risk of post-traumatic hip osteoarthritis?
Mario Cahueque, Marcos Martínez, Andrés Cobar...
https://pubmed.ncbi.nlm.nih.gov/29062212Actively Recruiting
Led by Unity Health Toronto · Updated on 2025-12-24
104
Participants Needed
1
Research Sites
52 weeks
Total Duration
This research aims to compare two surgical treatments for acetabular (hip) fractures in patients aged 60 years and older. Managing these fractures in the elderly is challenging due to pre-existing health issues, osteoporosis, and higher mortality risk. The study focuses on evaluating pain and physical function outcomes following different surgical approaches in this population. Participants will receive either acute primary total hip arthroplasty (THA) combined with open reduction internal fixation (ORIF) during the same surgery or ORIF alone, based on the surgeon's decision. This is an observational cohort study conducted across multiple academic centers affiliated with the Canadian Orthopaedic Trauma Society. Follow-up visits occur at 6 weeks, 3, 6, 12, and 24 months after surgery. During the study, patients will complete questionnaires such as the Oxford Hip Score to measure pain and function, and the European Quality of Life-5 Dimensions (EQ-5D) to assess quality of life. Functional mobility will be evaluated using the Timed Up & Go Test. Additional measures include pain levels, opioid use, hospital stay length, discharge location, time to full weight-bearing, return to work and daily activities, and hospital readmission within 30 days.
CONDITIONS
Geriatric Acetabular fracTures: Open Reduction Internal Fixation Versus Replacement
You may qualify if you...
You will not qualify if you...
Complete this quick 3-step screening to check your eligibility
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Up to 30 days
Participants undergo surgery to treat their acetabular fracture with either total hip arthroplasty combined with open reduction internal fixation or open reduction internal fixation alone. Post-operative care includes hospital stay and initial recovery.
Daily assessments during hospital stay
Duration - Up to 24 months
Participants are followed up as per standard of care to monitor recovery and assess outcomes such as pain, mobility, and quality of life.
Visits at 6 weeks, 3, 6, 12, and 24 months
Total: 1 location
1
Unity Health Toronto - St Michael's Hospital
Toronto, Ontario, Canada, M5C 1R6
Actively Recruiting
C
Cassandra Tardif-Theriault, BKin
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
Have more questions? Get in touch with our team for quick support
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here
Mario Cahueque, Marcos Martínez, Andrés Cobar...
https://pubmed.ncbi.nlm.nih.gov/29062212Reza Firoozabadi, William W Cross, James C Krieg...
https://pubmed.ncbi.nlm.nih.gov/28497099Sebastian P Boelch, Martin C Jordan, Rainer H Meffert...
https://pubmed.ncbi.nlm.nih.gov/27511470Marc Hanschen, Sebastian Pesch, Stefan Huber-Wagner...
https://pubmed.ncbi.nlm.nih.gov/28534471Zachary Morison, Dirk Jan F Moojen, Aaron Nauth...
https://pubmed.ncbi.nlm.nih.gov/26335343Sonya Khurana, Tamar B Nobel, Justin S Merkow...
https://pubmed.ncbi.nlm.nih.gov/26161760Patrick D G Henry, Sam Si-Hyeong Park, J Michael Paterson...
https://pubmed.ncbi.nlm.nih.gov/29462122Robert V O'Toole, Emily Hui, Amit Chandra...
https://pubmed.ncbi.nlm.nih.gov/23719343Michael J Weaver, Raymond Malcolm Smith, David W Lhowe...
https://pubmed.ncbi.nlm.nih.gov/29373451Katharine Hamlin, Gabija Lazaraviciute, Michalis Koullouros...
https://pubmed.ncbi.nlm.nih.gov/28790471