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Spots Global Cancer Trial Database for ASPREE Cancer Endpoints Study

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Trial Identification

Brief Title: ASPREE Cancer Endpoints Study

Official Title: ASPREE Cancer Endpoints Study

Study ID: NCT01968798

Conditions

Cancer

Interventions

Aspirin
Placebo

Study Description

Brief Summary: The ASPREE Cancer Endpoint Study (ACES), an ancillary study of the ASPirin in the Prevention of Events in the Elderly (ASPREE) Study, will allow for the examination of the effect of daily low-dose aspirin (100 mg) compared to placebo, on specific DNA biomarkers and selected specific incident and recurrent cancer and metastases. The establishment of this ACES biobank will allow for the exploration of DNA-related molecular mechanisms of aspirin's protective effect against cancer, cancer associated mortality and metastases, using blood or saliva DNA specimens, urine, and tumor tissue.

Detailed Description: The ASPREE Cancer Endpoint Study (ACES) is an ancillary study of the ASPirin in the Prevention of Events in the Elderly (ASPREE) Study, a 5 year randomized placebo- controlled trial of 100 mg of daily aspirin in 19,000 elderly in Australia and the US to determine whether the benefits of low dose daily aspirin outweigh the bleeding risks. The primary outcome of ASPREE is defined as prolongation of "disability-free life", measured as survival without physical disability or dementia. At present, the primary purpose of ACES is to: 1) collect information about participant cancer screenings, cancer diagnosis, and family history of cancer and to 2) establish a biologic specimen repository (biobank) for DNA and tumor tissue, and urine from the ASPREE large healthy aging population in the US and Australia for future use by ASPREE, NIA and NCI investigators, and academicians from the broader research community. At a time in the future and under separate application, the stored blood or saliva, urine, and tumor tissue, together with other information obtained about these participants (in relation to their health, lifestyle and other circumstances) will be analyzed to address specific questions regarding the association of biomarkers and major health outcomes including cancer.

Eligibility

Minimum Age: 65 Years

Eligible Ages: OLDER_ADULT

Sex: ALL

Healthy Volunteers: Yes

Locations

The University of Alabama at Birmingham, Birmingham, Alabama, United States

Palo Alto Medical Foundation Research Institute, Palo Alto, California, United States

Howard University, Washington, District of Columbia, United States

University of Florida Department of Aging and Geriatrics, Gainesville, Florida, United States

Morehouse School of Medicine, Atlanta, Georgia, United States

Emory/ Atlanta VAMC, Atlanta, Georgia, United States

Georgia Health Sciences University, Augusta, Georgia, United States

Rush Alzheimer's Disease Center, Chicago, Illinois, United States

University of Iowa, Iowa City, Iowa, United States

Kansas University Medical Center, Kansas City, Kansas, United States

Baton Rouge General, Baton Rouge, Louisiana, United States

Pennington Biomedical Research Center, Baton Rouge, Louisiana, United States

Mary Bird Perkins Our Lady of the Lake Cancer Center, Baton Rouge, Louisiana, United States

Mary Bird Perkins St. Tammany Parish Hospital, Covington, Louisiana, United States

Mary Bird Perkins Terrebonne General Hospital, Houma, Louisiana, United States

LSU Health Sciences- New Orleans, New Orleans, Louisiana, United States

Tulane Medical Center, New Orleans, Louisiana, United States

LSU Health Sciences- Shreveport, Shreveport, Louisiana, United States

University of Michigan, Ann Arbor, Michigan, United States

Wayne State University, Detroit, Michigan, United States

Henry Ford Health System, Detroit, Michigan, United States

Detroit Clinical Research Center, Novi, Michigan, United States

HealthPartners Research Institute, Minneapolis, Minnesota, United States

Phalen Village Clinic, Saint Paul, Minnesota, United States

Central Jersey Medical Center, Elizabeth, New Jersey, United States

New Jersey Medical College, Newark, New Jersey, United States

SUNY Downstate Medical Center, Brooklyn, New York, United States

Winthrop University Hospital, Mineola, New York, United States

Queens Cancer Medical Center, Queens, New York, United States

Wake Forest University Baptist Medical Center, Greensboro, North Carolina, United States

The Brody School of Medicine at ECU, Greenville, North Carolina, United States

Albert Einstein Medical Center, Philadelphia, Pennsylvania, United States

University of Pittsburgh Health Sciences Research Center, Pittsburgh, Pennsylvania, United States

Memorial Hospital of Rhode Island, Pawtucket, Rhode Island, United States

University of Tennessee Health Science Center, Memphis, Tennessee, United States

Meharry Medical College, Nashville, Tennessee, United States

University of Texas Southwestern Medical Center at Dallas, Dallas, Texas, United States

University of TX Medical Branch, Galveston, Texas, United States

Regional Academic Health Center, Harlingen, Texas, United States

UT Health Science Center at San Antonio, San Antonio, Texas, United States

Contact Details

Name: Anne Murray, MD, MSc

Affiliation: Berman Center

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

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