Permission to Collect Blood Over Time for Research

Not Recruiting

Trial ID: NCT00767234

Purpose

To determine whether biomarkers assessed in blood samples can be used to detect individuals at risk for developing blood clots or worsening of their underlying disease. The ultimate goal of the study is to identify key biomarkers derived from blood that are most characteristic and informative of individuals who will go on to develop a clotting complication.

Official Title

Predicting DVT Risk in GI Cancer Patients Using Plasma Biomarkers

Stanford Investigator(s)

George A. Fisher Jr.
George A. Fisher Jr.

Colleen Haas Chair in the School of Medicine

Lawrence "Rusty" Hofmann, MD
Lawrence "Rusty" Hofmann, MD

Professor of Radiology (Interventional Radiology)

Eligibility


Inclusion Criteria:

   - Male or female, >= 18 years old. There are no ethnic restrictions.

   - Active cancers of the GI tract (gastroesophageal, colorectal, or pancreatic-biliary)
   that have completed TNM staging by the American Joint Committee on Cancer; stage III
   disease if diagnosed within 2 months and all stage IV disease

   - Ability to understand and the willingness to sign a written informed consent document.

   - Existing staging CT imaging study

Exclusion Criteria:

   - Life expectancy < 6 months

   - History of deep vein thrombosis (DVT) or pulmonary embolism (PE)

   - Known pregnancy or positive urine pregnancy test in pre-menopausal women

   - On anticoagulant therapy (heparin, warfarin, direct thrombin inhibitors)

   - No CT imaging studies, or contraindications to undergoing CT imaging

   - Existing or anticipated need for a tunneled central venous catheter

   - Clinic visitation to Stanford Cancer center for secondary consultation purposes only

   - Inability to give informed consent

Intervention(s):

procedure: Observation

Not Recruiting

Contact Information

Stanford University
School of Medicine
300 Pasteur Drive
Stanford, CA 94305
CCTO
650-498-7061

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