Spots Global Cancer Trial Database for The Sanderson Study: A Case Control Study for the Development of Multiomics Blood Tests for Cancer Screening
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Trial Identification
Brief Title: The Sanderson Study: A Case Control Study for the Development of Multiomics Blood Tests for Cancer Screening
Official Title: The Sanderson Study: A Diagnostic Case-Control Study for the Development of Multiomics Blood Tests for Cancer Screening in a Real World Setting
Study ID: NCT05516927
Interventions
Study Description
Brief Summary: 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.
Detailed Description:
Eligibility
Minimum Age: 30 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: Yes
Locations
Crisp Regional Hospital, Cordele, Georgia, United States
Silver Cross Hospital and Medical centers, Orland Park, Illinois, United States
Margaret Mary, Batesville, Indiana, United States
Winona Health System, Winona, Minnesota, United States
Carroll County Memorial Hospital, Carrollton, Missouri, United States
Hannibal Regional Hospital, Hannibal, Missouri, United States
University Health Truman Medical Center, Kansas City, Missouri, United States
North Kansas City Hospital, North Kansas City, Missouri, United States
Renown Regional Medical Center, Reno, Nevada, United States
Inspira Medical Center, Mullica Hill, New Jersey, United States
St Joseph University, Paterson, New Jersey, United States
Iredell Memorial Hospital, Statesville, North Carolina, United States
Oregon Health and Science University, Portland, Oregon, United States
Geisinger Bloomsburg Hospital, Bloomsburg, Pennsylvania, United States
MacLeod Center for Cancer Treatment and Research, Florence, South Carolina, United States
Contact Details
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