Status:

COMPLETED

Special Drug Use Investigation for Arixtra® (Fondaparinux) Venous Thromboembolism Treatment

Lead Sponsor:

GlaxoSmithKline

Conditions:

Ataxia

Eligibility:

All Genders

Brief Summary

The purpose of this post-marketing surveillance study is to collect and assess information on safety and efficacy of fondaparinux injection in patients with venous thromboembolism (VTE). ("Arixtra" i...

Eligibility Criteria

Inclusion

  • Patients with acute pulmonary thromboembolism or acute deep venous thrombosis
  • Fondaparinux injection must be prescribed for the first time

Exclusion

  • Not applicable

Key Trial Info

Start Date :

January 1 2012

Trial Type :

OBSERVATIONAL

Allocation :

ACTUAL

End Date :

June 1 2015

Estimated Enrollment :

200 Patients enrolled

Trial Details

Trial ID

NCT01428531

Start Date

January 1 2012

End Date

June 1 2015

Last Update

July 15 2015

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Special Drug Use Investigation for Arixtra® (Fondaparinux) Venous Thromboembolism Treatment | DecenTrialz