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CompletedNCT03404635

Monotherapy Anticoagulation To Expedite Home Treatment of Venous Thromboembolism

Monotherapy Anticoagulation To Expedite Home Treatment of Venous

Status
Completed
Phase
Study type
Observational
Enrollment
1,300 (actual)
Sponsor
Indiana University · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Prospective, multicenter observational study, of the effectiveness of a standard of care protocol implemented to enhance home treatment of VTE. Study population will be selected as part of usual care as eligible for home treatment. Study personnel will travel to participating institutions to qualify the sites, deliver a Powerpoint® lecture to introduce the protocol, meet and train site principal investigators, emergency physicians and research personnel on the implementation of the protocol as part of usual clinical care, and data collection methods for a quality assurance registry with plans to use the data collected in this registry in future publications. Follow-up will be 30 days using medical records and/or telephone interview to assess for primary outcomes of bleeding or VTE recurrence.

Conditions

Interventions

TypeNameDescription
DRUGApixabanApixaban as standard of care for VTE
DRUGRivaroxabanRivaroxaban as standard of care for VTE

Timeline

Start date
2017-08-04
Primary completion
2020-05-08
Completion
2020-05-08
First posted
2018-01-19
Last updated
2020-08-07

Locations

2 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT03404635. Inclusion in this directory is not an endorsement.

Monotherapy Anticoagulation To Expedite Home Treatment of Venous Thromboembolism (NCT03404635) · Clinical Trials Directory