Actively Recruiting
Total Cancer Care Protocol: A Lifetime Partnership With Patients Who Have or May be at Risk of Having Cancer
Led by New Mexico Cancer Research Alliance · Updated on 2025-05-22
47500
Participants Needed
1
Research Sites
52 weeks
Total Duration
On this page
Sponsors
N
New Mexico Cancer Research Alliance
Lead Sponsor
H
H. Lee Moffitt Cancer Center and Research Institute
Collaborating Sponsor
AI-Summary
What this Trial Is About
Researchers are conducting an observational study to create an improved standard of cancer care by supporting new cancer research, clinical trials, technology, informatics solutions, and personalized medicine through the University of New Mexico Comprehensive Cancer Center and the Oncology Research Information Exchange Network Consortium. The study focuses on collecting and maintaining a large collection of biological samples and data from patients with cancer or at risk of cancer. This research is not a treatment trial but aims to build a centralized data and tissue repository for long-term use. Participants provide permission for their survey answers, medical records, cancer registry data, and biological samples such as blood and tissue collected during planned surgeries, diagnostic biopsies, or previous procedures to be used for research. Additional tumor samples may be collected during diagnostic procedures if available. This protocol involves ongoing collection and storage of clinical and related data from the time of enrollment and continues throughout the participant's lifetime. During the study, participants will provide biological specimens and data that will be linked to their clinical records for research purposes. Researchers will collect demographic information, medical treatment histories, and outcomes to build a comprehensive repository for up to 20 years. This study involves no treatment administration, and participants will be monitored through their regular clinical care while contributing data and samples for research.
CONDITIONS
Brief Title
Total Cancer Care Protocol: 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
- Has a diagnosis of cancer or is suspected of having cancer
- Able to understand and sign the Informed Consent form directly
- Pregnant women are permitted to be enrolled
You will not qualify if you...
- Prisoners
AI-Screening
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Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Up to 20 years
Participants provide permission for collection and study of biological samples and clinical data during routine care. This includes collection of blood, tissue, and other biological samples, as well as survey and medical records data for research purposes.
Visits occur as part of routine clinical care; additional sample collections may occur at the time of planned surgeries or biopsies
Trial Site Locations
Total: 1 location
1
University of New Mexico Comprehensive Cancer Center
Albuquerque, New Mexico, United States, 87102
Actively Recruiting
Research Team
C
Christine Serway, PhD
E
Ellen Wojcik, MBA-HCM
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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