This protocol is a prospective, case-control multi-center diagnostic study to assess the sensitivity and specificity of blood-based screening tests for the early detection of multiple cancers.
Study Type
OBSERVATIONAL
Enrollment
788
Participants who provide informed consent, meet the eligibility criteria and provide a blood sample for this study will be enrolled.
Crisp Regional Hospital
Cordele, Georgia, United States
Comparison of Blood Samples from Cancer Case and Non-cancer Control Participants
To compare blood samples from cancer case and non-cancer control subjects in order to develop and characterize blood-based multiomics tests in specific cancer types or in a combination of multiple cancers.
Time frame: 12 months
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