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NCT01691495

ARIXTRA® Adherence in SVT Patients.

ARIXTRA® Physician Adherence to the Prescribing Information in Isolated Superficial Vein Thrombosis (SVT) Patients.
GlaxoSmithKline·ClinicalTrials.gov·drugCompleted
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Study focus
Disease/Condition
Thrombosis, Venous
Drug/Device/Intervention
Fondaparinux
Study type
Observational
Intervention type
drug
Sponsor & location
Primary sponsor
GlaxoSmithKline
Timeline & enrollment
Phase
N/A
Start date
Oct 01, 2012
End date
Aug 01, 2014
Enrollment
1 participants
Primary outcome

The primary outcome will be a measure of physician adherence.

Summary

Fondaparinux is an anticoagulant used in the prevention and treatment of thromboembolic
 disease. It has recently been approved in the European Union (EU) for the treatment of
 patients with isolated superficial vein thrombosis (SVT), i.e. without concomitant deep vein
 thrombosis (DVT), of the lower limbs. As part of EU approval, GlaxoSmithKline (GSK) committed
 to evaluate physicians' adherence to fondaparinux prescribing information regarding proper
 diagnosis and dosing for the treatment of SVT.
 
 The primary objective is to evaluate physicians' adherence to fondaparinux prescribing
 information for the treatment of patients with SVT without concomitant DVT.
 
 The study is designed as a non-interventional, retrospective chart review of patients
 prescribed fondaparinux to treat their SVT. The study will be conducted in several EU
 countries.
 
 ARIXTRA® is a registered trademark of the GlaxoSmithKline group of companies.

ICD-10 classifications
Other venous embolism and thrombosisEmbolism and thrombosis of unspecified veinEmbolism and thrombosis of other specified veinsPerianal venous thrombosisArterial embolism and thrombosis
Data source
Registry
ClinicalTrials.gov
Trial ID
NCT01691495
Type
Non-Device Trial
About this record

Access comprehensive clinical trial information for NCT01691495 through Pure Global AI's free database. This phase not specified trial is sponsored by GlaxoSmithKline and is currently Completed. The study focuses on Thrombosis, Venous. Target enrollment is 1 participants.

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