Prostate Cancer Clinical Trial
Official title:
Genetic Investigation of Solid Tumors Cohort
The objective of this study is to obtain blood samples, solid tumor and/or benign hyperplasia samples to learn more about genetic differences that are linked to the formation of solid tumors.
Status | Completed |
Enrollment | 25 |
Est. completion date | May 2014 |
Est. primary completion date | May 2014 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: 1. Age 18 years or older 2. Eligible to have their blood drawn 3. Be reliable, cooperative and willing to comply with all protocol-specified procedures 4. Able to understand and grant informed consent 5. Diagnosis of a solid tumor Exclusion Criteria: 1. Has a significant chronic medical condition which would potentially confound interpretation of the individual's phenotype. 2. Treatment with any investigational agents or devices within thirty days preceding enrollment in the study. 3. Been administered or taken any CNS sedatives or depressants in the 12 hours prior to informed consent process |
Observational Model: Cohort
Country | Name | City | State |
---|---|---|---|
United States | Scripps Health | San Diego | California |
Lead Sponsor | Collaborator |
---|---|
Scripps Translational Science Institute |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Solid tumor biological insights | Obtain blood samples, solid tumor and/or benign hyperplasia samples, and in some instances normal tissue in order to gain biological insights into cancer (solid tumors) through population genetics and genomics. | Study completion | No |
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