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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT00830557
Other study ID # 354-06
Secondary ID P50CA102701-08CD
Status Recruiting
Phase
First received
Last updated
Start date October 2000
Est. completion date September 2024

Study information

Verified date July 2023
Source Mayo Clinic
Contact Adriana Delgado, CCRP
Phone 1-800-914-7962
Email pancreas@mayo.edu
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

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.


Description:

OBJECTIVES: Primary - 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. Secondary - 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.


Recruitment information / eligibility

Status Recruiting
Enrollment 12000
Est. completion date September 2024
Est. primary completion date September 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years to 120 Years
Eligibility DISEASE CHARACTERISTICS: - Diagnosis or suspicion of at least one of the following: - Pancreatic cancer - Pancreatic mass - Islet cell tumor PATIENT CHARACTERISTICS: - Able to understand and read English - Mentally competent and able to provide informed consent - Has not donated blood within the past 8 weeks PRIOR CONCURRENT THERAPY: - At least 7 days since prior blood transfusion - At least 7 days since prior surgery

Study Design


Intervention

Other:
medical chart review
baseline, 12 month and 36 months
survey administration
baseline, 6 month, 12 month
biospecimen collection
baseline

Locations

Country Name City State
United States Mayo Clinic Cancer Center Rochester Minnesota

Sponsors (2)

Lead Sponsor Collaborator
Mayo Clinic National Cancer Institute (NCI)

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Collection of clinical data, health and family histories by survey baseline enrollment, 6 months, 12 months
Primary Collection of blood and/or tissue, fecal and oral specimens baseline
Primary Collection of information regarding food preparation and intake by survey baseline
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