Actively Recruiting
A Lifetime Partnership With Patients Who Have or May be at Risk of Having Cancer
Led by University of Colorado, Denver · Updated on 2025-11-10
20000
Participants Needed
6
Research Sites
1145 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This is not a treatment study. The overall objective is to develop an improved standard of care through studying blood, tissue, biological, etc. samples, that patients have allowed researchers to procure.
CONDITIONS
Official Title
A Lifetime Partnership With Patients Who Have or May be at Risk of Having Cancer
Who Can Participate
Eligibility Criteria
You may qualify if you...
- 18 years of age and older
- Diagnosed with cancer or may be at risk for cancer
- Able to understand and sign the informed consent and research authorization form themselves or through a legally authorized representative
- Non-English speakers may participate using a short-form consent process
You will not qualify if you...
- Neonates (birth to 30 days old)
- Children under 18 years old
- Wards of the State
- Prisoners or those on probation or alternate sentencing
- Individuals unable to provide informed consent due to cognitive impairment or other reasons
- Adults or children who require proxy consent or are consenting in life-threatening situations
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 6 locations
1
University of Colorado Hospital
Aurora, Colorado, United States, 80045
Actively Recruiting
2
UCHealth Memorial Hospital Central
Colorado Springs, Colorado, United States, 80909
Actively Recruiting
3
UCHealth Memorial Hospital North
Colorado Springs, Colorado, United States, 80909
Actively Recruiting
4
Cherry Creek Medical Center
Denver, Colorado, United States, 80206
Actively Recruiting
5
UCHealth Poudre Valley Health System
Fort Collins, Colorado, United States, 80528
Actively Recruiting
6
Highlands Ranch Medical Center
Highlands Ranch, Colorado, United States, 80126
Actively Recruiting
Research Team
K
Kyra Anderson
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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