Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
1500 participants
OBSERVATIONAL
2004-06-30
2019-06-30
Brief Summary
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Detailed Description
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You will also have around 2 ½ tablespoons of blood drawn for special tests. These tests will look for any biologic factors associated with certain cancers. The interview and blood draw will be scheduled at the time and place of your convenience. You will not be informed of the results of any of the testing done with your samples.
There is a possibility that you might be contacted in the future about if researchers need clarification on any of information already collected. You are free to refuse any further participation if you wish.
This is an investigational study. Up to 1,500 participants will take part in this study.
Conditions
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Study Design
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CASE_CONTROL
PROSPECTIVE
Study Groups
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Control
Person with no history of cancer.
Questionnaire
50 Minute Interview
Interventions
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Questionnaire
50 Minute Interview
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
2. Willing and able to complete an administered questionnaire
3. Willing and able to donate 30 mL of blood
Exclusion Criteria
2. Individuals under the age of 18
18 Years
ALL
Yes
Sponsors
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National Cancer Institute (NCI)
NIH
National Institutes of Health (NIH)
NIH
M.D. Anderson Cancer Center
OTHER
Responsible Party
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Principal Investigators
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Carrie Daniel-MacDougall, PHD
Role: PRINCIPAL_INVESTIGATOR
M.D. Anderson Cancer Center
Locations
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University of Texas MD Anderson Cancer Center
Houston, Texas, United States
Countries
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Related Links
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UT MD Anderson Cancer Center website
Other Identifiers
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