Pilot Dose Finding and Pharmacokinetic Study of Fondaparinux in Children With Thrombosis

Completed · Phase 1

Conditions studied: Thrombosis, Heparin-induced Thrombocytopenia

In brief

This study will evaluate the use of a blood thinner, fondaparinux, which is approved for use in adults (not in children) in a children aged 1-18 years. Subject with a blood clot (thrombosis) or heparin-induced thrombocytopenia who need to be on a blood thinner will be eligible to participate. Subjects will receive a once daily dose of fondaparinux followed by blood tests at 2, 4, 12, and 24 hours after the first dose in order to determine the proper dose for this age group. The hypothesis is that children receiving fondaparinux will be able to receive a once daily dose. The currently available alternative agent, enoxaparin, needs to be given twice daily. In addition, an evaluation of the safety of this medication will be made by assessing for side effects, especially bleeding.

Key facts

Study ID
NCT00412464
Run by
Children's Hospital Los Angeles
People needed
24
Starts
2006-09-01
Expected to finish
2009-12-01
Last updated by the study team
2015-04-15

Who can join

Age: 1 and older, up to 18. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

You may not qualify if…

Where it is running

Full record on ClinicalTrials.gov

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