Status:
WITHDRAWN
Defining the Pathophysiology of Heterotopic Ossification: A Prospective Study
Lead Sponsor:
Vanderbilt University Medical Center
Conditions:
Heterotopic Ossification
Eligibility:
All Genders
Up to 70 years
Brief Summary
Our overarching aim is to define the pathophysiology, epidemiology, and natural history of HO by following patients from date of injury until full wound healing has occurred and the window for HO has ...
Detailed Description
The aforementioned general inclusion/exclusion criteria will be used to determine patient eligibility. All eligible patients will be identified using a patient list from StarPanel provided by the mana...
Eligibility Criteria
Inclusion
- Arm 1- Injured Patients
- Any patient treated in our hospital system from initial IRB approval until we reach our enrollment quota that are diagnosed with HO, hip fracture, midshaft/distal femur fracture, humerus fracture, proximal radius fracture, and elbow dislocation/fracture. This includes patients in all age groups and of all genders.
- Patients with a diagnosis of HO, hip fracture, midshaft/distal femur fracture, humerus fracture, proximal radius fracture, or elbow fracture must be receiving operative treatment for their injury.
- Patients with concurrent trauma will be grouped into a sub-analysis.
Exclusion
- Patients with pathologic fractures.
- Non-operative patients other than elbow dislocation patients
- Pregnant Women
- Patients who do not intend to follow-up at Vanderbilt
- Arm 2- Healthy Volunteers
- Inclusion Criteria:
- Volunteers (male or female) between ages of 18-70
- Weight greater than 110lbs
Key Trial Info
Start Date :
June 1 2022
Trial Type :
OBSERVATIONAL
Allocation :
ACTUAL
End Date :
June 1 2024
Estimated Enrollment :
Patients enrolled
Trial Details
Trial ID
NCT04867018
Start Date
June 1 2022
End Date
June 1 2024
Last Update
March 9 2022
Active Locations (1)
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1
Vanderbilt Children's Orthopaedics
Nashville, Tennessee, United States, 37232