Enoxaparin Versus Aspirin in Patients With Cancer and Stroke

NACompletedINTERVENTIONAL
Enrollment

20

Participants

Timeline

Start Date

December 18, 2012

Primary Completion Date

April 3, 2019

Study Completion Date

April 3, 2019

Conditions
Cancer Patients First-ever Acute Ischemic Stroke
Interventions
DRUG

Enoxaparin

Patients will be receive 6 months of subcutaneous enoxaparin (1 mg/kg BID with a maximum starting dose of 100 mg BID. Patients who weigh more than 100 kg will start at a dose of 100 mg BID; their subsequent dosing will be guided by hematology and may change.

DRUG

Aspirin

Patients will receive 6 months of oral aspirin (81 mg per day unless a higher dose is preferred by study physicians although the maximum acceptable dose will be 325 mg per day).

Trial Locations (7)

10065

Memorial Sloan Kettering Cancer Center, New York

New York Presbyterian Hospital, New York

10604

Memorial Sloan Kettering West Harrison, Harrison

11725

Memorial Sloan Kettering Cancer Center at Commack, Commack

07920

Memorial Sloan Kettering at Basking Ridge, Basking Ridge

Unknown

Columbia University, New York

Weill Cornell Medical Center, New York

All Listed Sponsors
collaborator

New York Presbyterian Hospital

OTHER

collaborator

Weill Medical College of Cornell University

OTHER

lead

Memorial Sloan Kettering Cancer Center

OTHER

NCT01763606 - Enoxaparin Versus Aspirin in Patients With Cancer and Stroke | Biotech Hunter | Biotech Hunter