The Use of Fondaparinux in Preventing Thromboembolism in High Risk Trauma Patients

PHASE2/PHASE3CompletedINTERVENTIONAL
Enrollment

105

Participants

Timeline

Start Date

December 31, 2007

Primary Completion Date

June 30, 2008

Study Completion Date

June 30, 2008

Conditions
Venous Thromboembolism
Interventions
DRUG

fondaparinux sodium

fondaparinux 2.5mg SubQ daily for DVT prophylaxis to be started by treating physicians once deemed safe and to be discontinued once patient in discharged from the hospital or at discretion of treating physicians.

DEVICE

sequential compression devices

Sequential compression devices at all times during the patient's hospital admission will be used in patients who have a contraindication to pharmacologic DVT prophylaxis. This is already the current standard of care.

Trial Locations (1)

94143

San Francisco General Hospital, San Francisco

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

GlaxoSmithKline

INDUSTRY

lead

Mary Knudson, M.D.

OTHER