Bladder Cancer Clinical Trial

Permission to Collect Blood Over Time for Research

Summary

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.

View Eligibility Criteria

Eligibility Criteria

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

Study is for people with:

Bladder Cancer

Estimated Enrollment:

104

Study ID:

NCT00767234

Recruitment Status:

Terminated

Sponsor:

Stanford University

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There is 1 Location for this study

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Stanford University School of Medicine
Stanford California, 94305, United States

How clear is this clinincal trial information?

Study is for people with:

Bladder Cancer

Estimated Enrollment:

104

Study ID:

NCT00767234

Recruitment Status:

Terminated

Sponsor:


Stanford University

How clear is this clinincal trial information?

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