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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ENROLLING_BY_INVITATION
5000 participants
OBSERVATIONAL
2008-09-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Blood Draw
blood draw, bone marrow procedure, or tissue biopsy
Interventions
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blood draw, bone marrow procedure, or tissue biopsy
Eligibility Criteria
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Inclusion Criteria
* Male or female of all ages
* Willing and able to sign informed consent
* Willing guardian consent for participants under 18 years of age
Exclusion Criteria
1 Year
ALL
No
Sponsors
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National Institutes of Health (NIH)
NIH
National Cancer Institute (NCI)
NIH
OHSU Knight Cancer Institute
OTHER
Responsible Party
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Marc Loriaux
Associate Professor
Principal Investigators
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Marc Loriaux, MD
Role: PRINCIPAL_INVESTIGATOR
OHSU Knight Cancer Institute
Locations
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OHSU Knight Cancer Institute
Portland, Oregon, United States
Countries
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Other Identifiers
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IRB00004422
Identifier Type: -
Identifier Source: org_study_id
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