MedPath

Enoxaparin Versus Aspirin in Patients With Cancer and Stroke

Not Applicable
Completed
Conditions
Cancer Patients First-ever Acute Ischemic Stroke
Interventions
Registration Number
NCT01763606
Lead Sponsor
Memorial Sloan Kettering Cancer Center
Brief Summary

Patients with cancer who develop stroke are at high risk for future strokes or other clotting events. These patients are routinely treated with medicines that thin their blood, including enoxaparin or aspirin. However, it is unclear which medicine is best and whether these medicines can be adequately studied in a clinical trial.

The purpose of this Phase I/II study is to determine if a clinical trial of different blood thinners in patients with cancer and stroke is possible. In addition, the study aims to compare the effects, good and/or bad, of enoxaparin with those of aspirin on patients with cancer and recent stroke.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
20
Inclusion Criteria
  • 18 to 85 years of age.
  • Active cancer, defined as a pathologic diagnosis of or treatment for any cancer, other than basal-cell or squamous-cell carcinoma of the skin, within the past six months; or patients with known recurrent or metastatic disease within the past six months.
  • A pathology report issued at the enrolling site confirming the diagnosis of cancer is required for enrollment.
  • Acute ischemic stroke within the prior four weeks, defined as a new neurologic deficit(s) with MRI evidence of acute ischemia in a referable location, and no clinical or radiologic indication of a non-cerebrovascular mimic, such as a brain metastasis, as the etiology of the deficit(s).
Exclusion Criteria
  • Inability to get brain MRI
  • Known malignant primary brain tumor.
  • Diagnosis of intracranial hemorrhage within the past 3 months, including intratumoral hemorrhage into brain metastases from a systemic cancer.
  • Active or serious bleeding within two weeks of enrollment.
  • Patient condition associated with a high risk of bleeding such as recent surgery or peptic ulcer disease.
  • Clear indication for anticoagulation (e.g., atrial fibrillation) anticipated during the study period.
  • Clear indication for antiplatelet agents (e.g., cardiac stents); a patient receiving aspirin for primary prevention prior to index stroke may be enrolled as long as study investigators believe it would be safe for the patient to stop aspirin if the patient was randomized to the enoxaparin arm.
  • Active bleeding diathesis.
  • Platelet count of ≤ 70,000/mm3, an international normalized ratio (INR) > 1.6, or a partial thromboplastin time (PTT) > 40 seconds.
  • Known allergy to heparin or aspirin or a history of heparin induced thrombocytopenia.
  • Serum creatinine > 2 mg/dl.
  • AST or ALT > 200 U/L.
  • Hemoglobin < 8 gm/dl
  • Symptomatic carotid stenosis.
  • Active pregnancy.
  • Life expectancy < 1 month or current hospice care
  • Unavailability for follow-up.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
AspirinAspirinPatients assigned to Aspirin.
EnoxaparinEnoxaparinPatients assigned to enoxaparin.
Primary Outcome Measures
NameTimeMethod
Safety Outcomes1 year

Number of Participants with intracranial hemorrhage, symptomatic intracranial hemorrhage, major bleeding, and death

Feasibility Outcomes6 months

The primary feasibility outcome is patient enrollment defined as the number of patients who enroll in the study divided by the number of patients who were eligible to enroll.

Secondary Outcome Measures
NameTimeMethod
Number of Participants With or Without Recurrent Ischemic Stroke6 months

Secondary efficacy outcomes will be assessed for and will include recurrent ischemic stroke, all strokes (ischemic or hemorrhagic), transient ischemic attack, myocardial infarction, deep vein thrombosis, pulmonary embolism, and systemic arterial thrombosis. Functional outcomes will also be evaluated, including the modified Rankin Scale score, the National Institute of Health Stroke Scale, and the Karnofsky Performance Status Scale.

Trial Locations

Locations (7)

New York Presbyterian Hospital

🇺🇸

New York, New York, United States

Memorial Sloan Kettering at Basking Ridge

🇺🇸

Basking Ridge, New Jersey, United States

Memorial Sloan Kettering West Harrison

🇺🇸

Harrison, New York, United States

Memorial Sloan Kettering Cancer Center at Commack

🇺🇸

Commack, New York, United States

Memorial Sloan Kettering Cancer Center

🇺🇸

New York, New York, United States

Columbia University

🇺🇸

New York, New York, United States

Weill Cornell Medical Center

🇺🇸

New York, New York, United States

© Copyright 2025. All Rights Reserved by MedPath