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HTRS TE Registry (ThromboEmbolism Registry)

NCT00266994 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 2760

Last updated 2013-02-21

No results posted yet for this study

Summary

The TE Registry is a multi-institutional bioinformatics database for the collection of data relevant to TE. Participating HTRS affiliated study centers may enroll patients and enter data in the TE Registry by completing enrollment and data entry forms and transmitting them to the study center. The purpose of this study is to improve our understanding of the epidemiology, pathophysiology, and outcome of patients suffering from thromboembolism (TE) events.

The initial objectives of the registry are:

* Evaluate the epidemiology and clinical characteristics of known prothrombotic risk factors in persons with TE.
* Identify the frequency and nature of complications associated with TE and its treatment.
* Describe the phenotypes and complications seen in persons with multiple molecular risk factors for TE.
* Compare the epidemiology, clinical characteristics, and complications seen in patients with and without known risk factors for TE.

Conditions

  • Thromboembolism

Sponsors & Collaborators

  • Hemophilia and Thrombosis Research Society

    collaborator UNKNOWN

  • Nationwide Children's Hospital

    lead OTHER

Principal Investigators

  • Bryce A Kerlin, MD · Nationwide Children's Hospital

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2005-12-31
Primary Completion
2012-10-31
Completion
2012-10-31

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00266994 on ClinicalTrials.gov