Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
690 participants
OBSERVATIONAL
2004-02-29
2011-12-31
Brief Summary
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Detailed Description
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* To utilize the PCRT clinical data base to perform clinicopathologic correlation with the results of those studies.
* To test new hypotheses as they emerge.
Conditions
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Study Design
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CASE_CONTROL
PROSPECTIVE
Interventions
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Serum and DNA Samples
To collect serum and DNA samples from subjects
Eligibility Criteria
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Inclusion Criteria
Criteria
4.1 At the time of subject registration, CRAB will verify the institution's IRB date to ensure that the subject can be enrolled.
4.2 Potential study participants must meet the eligibility criteria found in Section 12.0 (Eligibility Checklist). Candidates will fall into one of four groups:
1. Pancreatic cancer patients;
2. Pancreatic and Liver Disease patients;
3. Healthy, At-Risk Volunteers (smoker, (defined as individuals who have smoked \>= 100 cigarettes in their lifetime, and who currently smoke every day or some days \[MMWR November 12, 2004, 53(44);1035-1037\]), diabetic, and/or family history); and
4. Healthy Volunteers (no history of cancer). The Eligibility Checklist must be photocopied, completed and stored on site. Eligibility is confirmed during registration, by answering yes to the question, Have all eligibility criteria been met? on the Registration Form.
Eligibility Checklist:
1. Pancreatic Cancer Patient Criteria All subjects, regardless of gender and ethnicity are eligible for this study Pathological diagnosis of pancreatic malignant neoplasm Expected availability of clinical follow up data Eighteen years old or older All subjects must be informed of the investigational nature of this protocol Written, informed consent obtained in accordance with institutional and federal guidelines
2. Pancreatitis and Liver Disease Subject Criteria All subjects, regardless of gender and ethnicity are eligible for this study Pathological diagnosis of pancreatitis or liver disease Eighteen years old or older All subjects must be informed of the investigational nature of this protocol Written, informed consent obtained in accordance with institutional and federal guidelines
3. Healthy, At-Risk Volunteers All subjects, regardless of gender and ethnicity are eligible for this study Is a smoker, is diabetic AND/OR has a family history of pancreatic cancer Eighteen years old or older with no history of cancer All subjects must be informed of the investigational nature of this protocol Written, informed consent obtained in accordance with institutional and federal guidelines
4. Healthy Volunteers (no at-risk factors) All subjects, regardless of gender and ethnicity are eligible for this study Eighteen years old or older with no history of cancer All subjects must be informed of the investigational nature of this protocol Written, informed consent obtained in accordance with institutional and federal guidelines
18 Years
ALL
Yes
Sponsors
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Pancreatic Cancer Research Team
OTHER
Responsible Party
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Principal Investigators
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Manuel Hidalgo, MD, PhD
Role: STUDY_CHAIR
Hospital Universitario Sanchinarro, Madrid, Spain
Locations
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Scottsdale Healthcare
Scottsdale, Arizona, United States
University of Arizona/Arizona Cancer Center
Tucson, Arizona, United States
UCLA Medical Center
Los Angeles, California, United States
RUSH University Medical Center
Chicago, Illinois, United States
Sidney Kimmel Comprehensive Cancer Center/Johns Hopkins
Baltimore, Maryland, United States
Abbott Northwestern Hospital/Virginia Piper Cancer Institute
Minneapolis, Minnesota, United States
University of New Mexico
Albuquerque, New Mexico, United States
Sarah Cannon Research Institute
Nashville, Tennessee, United States
South Texas Oncology and Hematology
San Antonio, Texas, United States
University Hospital (12 De Octubre)
Madrid, , Spain
Countries
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Related Links
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Pancreatic Cancer Research Team - Public/Members
Other Identifiers
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PCRT 03 001
Identifier Type: -
Identifier Source: org_study_id
NCT00250107
Identifier Type: -
Identifier Source: nct_alias
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