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:
2025-12-24 @ 10:51 PM
Ignite Modification Date:
2025-12-24 @ 10:51 PM
NCT ID:
NCT04169269
Eligibility Criteria:
Inclusion Criteria:
* • Orthopaedic trauma patients deemed by the attending, treating surgeon to require an extended duration of venous thromboembolism chemoprophylaxis beyond that provided as an inpatient.
* Patients being discharged directly to home.
Exclusion Criteria:
* • Patients being discharged to a rehabilitation center or a skilled nursing facility.
* A contraindication to anticoagulation such as traumatic or other hemorrhage, as determined by the treating surgeon and/or consulting services.
* Ongoing venous thromboembolism treatment or extended prophylaxis (i.e. past history of multiple deep vein thrombosis/pulmonary embolism) for current or recent deep vein thrombosis, pulmonary embolism or other coagulopathic disorder
* Chronic anticoagulation for atrial fibrillation or other medical disorder requiring chronic anticoagulation therapy.
* Perceived low-risk patients requiring only aspirin or no pharmacological venous thromboembolism prophylaxis.
* Pregnant, prisoner, under 18 years old, or do not speak English
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT04169269
Study Brief:
Protocol Section:
NCT04169269