Collecting Medical Information and Tissue Samples From Patients With Pancreatic Cancer or Other Pancreatic Disorders
|The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details.|
|ClinicalTrials.gov Identifier: NCT00830557|
Recruitment Status : Recruiting
First Posted : January 28, 2009
Last Update Posted : September 11, 2017
RATIONALE: Gathering medical information and collecting and storing samples of blood and tissue to test in the laboratory may help doctors develop better ways to screen people at risk for pancreatic cancer or other pancreatic disorders in the future.
PURPOSE: This clinical trial is collecting medical information and tissue samples from patients with pancreatic cancer or other pancreatic disorders.
|Condition or disease||Intervention/treatment|
|Islet Cell Tumor Pancreatic Cancer Pancreatic Disease||Other: medical chart review Other: survey administration Other: biospecimen collection|
- To collect clinical data and family histories and blood and/or tissue samples from patients diagnosed with pancreatic diseases, including pancreatic cancer, for use in future studies.
- To collect information regarding food preparation and intake in these patients.
- To make available to researchers medical data and biospecimens to enable them to develop better ways to screen people at risk for pancreatic conditions, including pancreatic cancer.
- To investigate genes or substances that increase susceptibility of developing pancreatic conditions.
- To find agents that may help prevent, treat, or cure these conditions.
- To learn whether inherited factors increase the risk of pancreatic diseases, pancreatic cancer, or other cancers.
OUTLINE: This is a multicenter study.
Patients complete two 1-hour surveys assessing health, clinical and family history of pancreatic conditions including cancer, and food preparation and intake. Patients also complete a 15- to 30-minute follow up survey at 6 months and 1 year to assess health, health practices, and family history. A review of the patient's medical information is obtained from the medical record.
Blood samples are collected for future research studies. Oral cells and stool samples may also be collected for future studies.
|Study Type :||Observational|
|Estimated Enrollment :||7500 participants|
|Official Title:||Biospecimen Resource for Pancreas Research, a Data & Tissue Bank (Also Known as a Bio-repository, Bio-bank, Data & Tissue Database, Data & Tissue Registry, Etc.) to Help Advance Research in Pancreas Disease|
|Study Start Date :||October 2000|
|Estimated Primary Completion Date :||September 2022|
|Estimated Study Completion Date :||September 2022|
Other: medical chart review
- Collection of clinical data, health and family histories by survey [ Time Frame: baseline enrollment, 6 months, 12 months ]
- Collection of blood and/or tissue, fecal and oral specimens [ Time Frame: baseline ]
- Collection of information regarding food preparation and intake by survey [ Time Frame: baseline ]
Biospecimen Retention: Samples With DNA
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00830557
|Contact: Shayna Amosfirstname.lastname@example.org|
|Contact: Bridget Eversmanemail@example.com|
|United States, Minnesota|
|Mayo Clinic Cancer Center||Recruiting|
|Rochester, Minnesota, United States, 55905|
|Contact: Clinical Trials Office - All Mayo Clinic Locations 507-538-7623|
|Principal Investigator:||Gloria M. Petersen, PhD, FACMG||Mayo Clinic|