Detecting Abnormal Blood Clotting in Patients With Metastatic Cancer Undergoing Surgery
Thromboembolism, Unspecified Adult Solid Tumor, Protocol Specific
About this trial
This is an observational trial for Thromboembolism focused on measuring thromboembolism, unspecified adult solid tumor, protocol specific
Eligibility Criteria
DISEASE CHARACTERISTICS: Patients meeting the following criteria: Diagnosis of metastatic carcinoma Must be enrolled in 1 of the following surgical protocols: NCI-99-C-0123 NCI-00-C-0069 NCI-03-C-0085 NCI-03-C-0212 Healthy control participant* meeting the following criteria: No anemia or thrombocytopenia No history of venous thromboembolism (deep vein thrombosis, pulmonary emboli) No history of coronary artery disease or stroke No chronic inflammatory disease No diabetes mellitus Have not smoked tobacco within the past 6 months NOTE: * Selected on the basis of gender and age to match the patients as they are accrued PATIENT CHARACTERISTICS: No symptomatic infections or other acute illness within the past 14 days PRIOR CONCURRENT THERAPY: At least 3 days since prior drugs known to inhibit platelet function At least 7 days since prior acetylsalicylic acid No concurrent estrogen contraceptives or hormone replacement therapy No concurrent anticoagulants
Sites / Locations
- National Institutes of Health Clinical Center, 9000 Rockville Pike