Pancreatic Cancer Genetic Epidemiology (PACGENE) Study
2 other identifiers
observational
4,770
1 country
1
Brief Summary
The goal of this research study is to investigate the role of genes that may point to a higher risk of developing pancreatic cancer.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Jun 2002
Longer than P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
June 19, 2002
CompletedFirst Submitted
Initial submission to the registry
September 5, 2007
CompletedFirst Posted
Study publicly available on registry
September 10, 2007
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 1, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
June 1, 2025
CompletedJanuary 6, 2020
January 1, 2020
23 years
September 5, 2007
January 3, 2020
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Identification of susceptibility genes in high risk familial pancreatic cancer (FPC) pedigrees using cutting-edge genetic analysis methods
Data collection from patient response to 30-40 minute questionnaire and blood test.
8 Years
Study Arms (1)
Questionnaire
Pancreatic cancer patients or family member.
Interventions
Questionnaire taking about 30-40 minutes to complete.
Eligibility Criteria
MDACC pancreatic cancer patients and family members (two or more) of someone with pancreatic cancer, all over over the age of 18.
You may qualify if:
- \) An effected or uneffected member of a family, age 18 or older, that has two or more reported pancreatic cancers in the family.
You may not qualify if:
- Cases under age 18.
- Relatives of pancreatic cancer cases under age 18.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- M.D. Anderson Cancer Centerlead
- National Cancer Institute (NCI)collaborator
Study Sites (1)
University of Texas MD Anderson Cancer Center
Houston, Texas, 77030, United States
Related Links
Biospecimen
Blood sample will be collected.
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Carrie Daniel-MacDougall, PHD
M.D. Anderson Cancer Center
Study Design
- Study Type
- observational
- Observational Model
- CASE CONTROL
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
September 5, 2007
First Posted
September 10, 2007
Study Start
June 19, 2002
Primary Completion
June 1, 2025
Study Completion
June 1, 2025
Last Updated
January 6, 2020
Record last verified: 2020-01