Pancreatic Adenocarcinoma Gene Environment Risk Study
This observational study, called the Pancreatic Adenocarcinoma Gene Environment Risk Study, aims to understand the factors that contribute to pancreatic cancer. Researchers are collecting information and samples from people with pancreatic cancer and those with other conditions affecting the pancreas, liver, or intestines. There are no specific interventions or treatments being tested in this study. The goal is to gather data over 10 years to identify connections between genes, environment, and pancreatic cancer. The study is currently recruiting a large number of participants, up to 10,000 people. To join, you must be at least 18 years old and have either a confirmed diagnosis of pancreatic adenocarcinoma (a type of pancreatic cancer) or certain other pancreatic, liver, or intestinal conditions.
- Study design
- This is an observational study with a planned enrollment of up to 10,000 participants. It is not testing a specific drug or treatment.
- What's involved
- You will be asked to complete a medical/family history questionnaire and provide a blood sample. Some participants may also provide a urine sample, and researchers may save biological samples collected during clinical procedures for research. You will also be asked for permission to access your medical records and to be recontacted for updates.
- Compensation
- Not stated in the trial record.
- Follow-up
- The data will be used in cohort association studies, with endpoints measured at 10 years.
AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.
Pancreatic Adenocarcinoma Gene Environment Risk Study
At a glance
Conditions
Where it's being run
1 sites across 1 statesStudy leadership
- Randall E Brand, MD · PRINCIPAL_INVESTIGATOR · University of Pittsburgh
Who to contact
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Do you actually qualify for this trial?
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Inclusion
Exclusion
What this trial measures
- The data will be used in cohort association studies. Endpoints will depend on the number of patients in the study and the number of markers that are being evaluated.10 years