Actively Recruiting
Biospecimen Resource for Pancreas Disease to Help Advance Research in Pancreatic Cancer and Other Pancreatic Disorders
Led by Mayo Clinic ยท Updated on 2026-03-09
20000
Participants Needed
3
Research Sites
N/A
Total Duration
On this page
Sponsors
M
Mayo Clinic
Lead Sponsor
N
National Cancer Institute (NCI)
Collaborating Sponsor
AI-Summary
What this Trial Is About
Researchers are collecting medical information and tissue samples from patients who have pancreatic cancer or other pancreatic disorders. The purpose of this observational study is to create a resource of biospecimens and data to help discover and develop biomarkers for risk, early detection, and new targeted treatments for pancreatic diseases, especially pancreatic cancer. Participants provide blood, saliva, and leftover tissue samples for the study. They also complete questionnaires and have their medical records reviewed. Specimens and data are collected at different timepoints including baseline, 6 months, 12 months, and 36 months as part of the study process. During the study, patients will complete surveys about their health, family history, and food intake. Blood, tissue, fecal, and oral samples are collected. Medical charts are reviewed at baseline, 12 months, and 36 months. The study monitors these data and samples over time to support pancreas disease research. Participation involves regular assessments and data collection over at least a year.
CONDITIONS
Brief Title
Collecting Medical Information and Tissue Samples From Patients With Pancreatic Cancer or Other Pancreatic Disorders
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Known or suspected pancreas disease including pancreas adenocarcinoma
- Known or suspected pancreas disease including islet cell cancer
- Known or suspected pancreas disease including pancreatic cysts
- Known or suspected pancreas disease including hereditary, acute, or chronic pancreatitis
- Next of kin of a deceased participant who did not complete participation before passing away
- Age 18 years or older
You will not qualify if you...
- Under the age of 18
- Unable to provide informed consent
- Prison inmates
AI-Screening
AI-Powered Screening
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 - Baseline
Participants undergo blood, saliva, and previously obtained leftover tissue sample collection and complete questionnaires to provide clinical data, health, family histories, and dietary information.
1 visit (in-person)
Duration - Up to 36 months
Participants have their medical records reviewed and complete follow-up surveys to collect ongoing clinical data and health information.
Surveys and medical record reviews at 6, 12, and 36 months
Trial Site Locations
Total: 3 locations
1
Mayo Clinic Hospital in Arizona
Phoenix, Arizona, United States, 85054
Actively Recruiting
2
Mayo Clinic in Florida
Jacksonville, Florida, United States, 32224-9980
Actively Recruiting
3
Mayo Clinic in Rochester
Rochester, Minnesota, United States, 55905
Actively Recruiting
Research Team
A
Adriana Delgado, MA
H
Heather M Streich, CCRP
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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