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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RECRUITING
5000 participants
OBSERVATIONAL
2023-07-18
2038-12-31
Brief Summary
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Detailed Description
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Conditions
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Keywords
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Normal
Participants and donor samples without disease (ex: non-cancer)
No interventions assigned to this group
Disease state or condition
Participants and donor samples with known disease or condition (ex: cancer)
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* Able to donate a blood, urine, tissue, and/or other biospecimen sample
* Able to provide informed consent to participate in the study
Exclusion Criteria
* Individuals who lack the capacity to give informed consent
18 Years
ALL
Yes
Sponsors
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Vincere Cancer Center
OTHER
Responsible Party
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Principal Investigators
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Vershalee Shukla, MD
Role: PRINCIPAL_INVESTIGATOR
Vincere Cancer Center
Locations
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Vincere Cancer Center
Scottsdale, Arizona, United States
Countries
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Central Contacts
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Facility Contacts
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Christine Lau, MD
Role: primary
Other Identifiers
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VCC-BIOBANK-001
Identifier Type: -
Identifier Source: org_study_id