Summary

for people ages 18-99 (full criteria)
at Muscle Shoals, Alabama
study started
estimated completion

Description

Summary

The protocol is a large registry to describe acute, sub-acute and extended duration of anticoagulation management, clinical and economic duration of anticoagulation management, clinical and economic outcomes in patients with treated acute VTE (DVT and PE) in the real-world setting. Main objectives are to clarify the: - treatment related details for acute VTE (either conventional anticoagulation therapy, treatment with a direct oral anti-coagulant or other modalities of treatment) - Rate of early and late symptomatic VTE recurrence - Rate and nature of complications of VTE including post thrombotic syndrome and chronic thromboembolic pulmonary hypertension - Rate of bleeding complications - Rate of all-cause mortality at six months

Official Title

Global Anticoagulant Registry in the Field Observing Treatment and Outcomes in Patients With Treated Acute Venous Thromboembolic Events in the Real World

Details

Other objectives are to clarify the additional outcomes of:

  • Stroke (Measured by number of incidences)
  • Transient Ischemic Attack (TIA) (Measured by number on incidences)
  • ST Elevated Myocardial Infarction (STEMI) (Measured by number of incidences)
  • Non-ST Elevated Myocardial Infraction (NSTEMI) (Measured by number of incidences)
  • Unstable Angina (Measured by number of incidences)
  • Quality of life and patient reported outcomes and costs associated with the management of VTE.

Keywords

Venous Thromboembolism Deep Vein Thrombosis Pulmonary Embolism venous, thromboembolism, embolism, DVT, Pulmonary Embolism, thrombosis Thrombosis Thromboembolism Embolism Venous Thrombosis Anticoagulants

Eligibility

You can join if…

Open to people ages 18-99

  • Written informed consent
  • Age 18 years and over
  • Treated first time or recurrent DVT (lower or upper extremity), PE alone or overlapping DVT and PE confirmed by appropriate diagnostic methods (patients must be assessed for eligibility within 30 days of diagnosis)
  • Patients included with recurrent VTE must have completed treatment for the previous VTE episode

You CAN'T join if...

  • Patients for whom long-term follow-up is not envisaged within the enrolling hospital or the associated primary care physician
  • Patients participating in an interventional study that dictates treatments, visit frequency, or diagnostic procedures
  • Patients with only superficial vein thrombosis (SVT)

Location

  • Dr Terence Hart
    Muscle Shoals Alabama 35662 United States

Details

Status
accepting new patients
Start Date
Completion Date
(estimated)
Sponsor
Thrombosis Research Institute
Links
Global Anticoagulant Registry in the FIELD, Venous thromboembolism Event (GARFIELD-VTE)
Sign up for this study
ID
NCT02155491
Study Type
Observational [Patient Registry]
Last Updated