Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-25 @ 4:53 AM
Ignite Modification Date:
2025-12-25 @ 4:53 AM
NCT ID:
NCT04867018
Eligibility Criteria:
Arm 1- Injured Patients
Inclusion Criteria:
* 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 Criteria:
* 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
Exclusion Criteria:
* Chronic medical conditions such as diabetes, hypertension, high cholesterol, rheumatologic disorders, infections, etc.
* History of recent trauma or burn injury
* Recent inpatient admission within the last year
* Pregnant females or people on hormone replacement therapy
* People on any anticoagulant medication or NSAIDS
Sex:
ALL
Maximum Age:
70 Years
Study:
NCT04867018
Study Brief:
Protocol Section:
NCT04867018