Assessments for Cancer Risk
What You Need to Know Before You Apply
What is the purpose of this trial?
This trial aims to improve cancer care by studying samples, such as blood and tissue, from individuals with cancer or those at risk. Researchers will collect and analyze these samples and related data to advance medicine. The focus is not on testing new treatments but on gathering information to enhance future care. The trial seeks participants diagnosed with cancer or those who believe they might be at risk. As an unphased trial, this study offers participants the chance to contribute to valuable research that could shape the future of cancer care.
Do I need to stop my current medications for this trial?
The trial information does not specify whether you need to stop taking your current medications. Since this is not a treatment study, it's likely you can continue your medications, but you should confirm with the study team.
Why are researchers excited about this trial?
Researchers are excited about this trial because it focuses on gathering comprehensive data from patients who have or may be at risk for cancer. Unlike standard treatments that directly target cancer cells, this approach emphasizes the collection of blood, tissue, and other biological samples, along with detailed medical and survey data. This holistic dataset is crucial because it can lead to breakthroughs in understanding cancer, potentially paving the way for personalized medicine and more effective, tailored treatments in the future. By combining biospecimen collection with extensive data analysis, this trial aims to unlock new insights into cancer prevention and management.
Who Is on the Research Team?
Virginia Borges, MD
Principal Investigator
University of Colorado, Denver
Are You a Good Fit for This Trial?
Inclusion Criteria
Timeline for a Trial Participant
Screening
Participants are screened for eligibility to participate in the trial
Biospecimen and Data Collection
Collection of blood, tissue, and other biological samples along with associated data from patients with cancer or at risk of having cancer
Follow-up
Participants are monitored for safety and effectiveness after data collection
What Are the Treatments Tested in This Trial?
Interventions
- Biospeciman Collection
- Medical Chart Reviews
- Survey Assessments
How Is the Trial Designed?
1
Treatment groups
Experimental Treatment
Patients with cancer or who are at risk of having cancer who have given consent to have blood, tissue, other biological samples and their associated data (survey data, medical records data, cancer registry data, and other related data) collected and stored for the advancement of medicine.
Find a Clinic Near You
Who Is Running the Clinical Trial?
University of Colorado, Denver
Lead Sponsor
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