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2004-01
2027-12
2027-12
10000
NCT00912717
University of Pittsburgh
University of Pittsburgh
OBSERVATIONAL
Pancreatic Adenocarcinoma Gene Environment Risk Study
After informed consent, participants will be asked to complete a medical/family history questionnaire and provide a blood sample. Some participants may also be asked to provide a urine sample. Individuals undergoing procedures that require collection of biological samples for clinical purposes may have these samples saved for research purposes. Participants will also be asked for their permission for study investigators to access medical records and/or recontact them for updates to their medical and family histories. Data and biospecimens will be stored for potential future research projects.
N/A
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
| Study Registration Dates | Results Reporting Dates | Study Record Updates |
|---|---|---|
2009-06-01 | N/A | 2024-10-10 |
2009-06-02 | N/A | 2024-10-15 |
2009-06-03 | N/A | 2024-10 |
This section provides details of the study plan, including how the study is designed and what the study is measuring.
Primary Purpose:
N/A
Allocation:
N/A
Interventional Model:
N/A
Masking:
N/A
Arms and Interventions
| Participant Group/Arm | Intervention/Treatment |
|---|---|
| : Pancreatic Cancer individuals who have been diagnosed with pancreatic cancer | |
| : Unaffected individuals who have not been diagnosed with pancreatic cancer |
| Primary Outcome Measures | Measure Description | Time Frame |
|---|---|---|
| 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 |
| Secondary Outcome Measures | Measure Description | Time Frame |
|---|
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
|
Study Contact Name: Randall E Brand, MD Phone Number: 412-623-3105 Email: brandre@upmc.edu |
Study Contact Backup Name: Beth Dudley, MS, MPH, CGC Phone Number: 412-623-3105 Email: dudleyre@upmc.edu |
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person’s general health condition or prior treatments.
Ages Eligible for Study:
ALL
Sexes Eligible for Study:
18 Years
Accepts Healthy Volunteers:
1
This is where you will find people and organizations involved with this study.
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
General Publications
No publications available
