Recruitment

Recruitment Status
Recruiting
Estimated Enrollment
50

Summary

Conditions
  • Familial Atypical Multiple Mole Melanoma
  • BRCA 1/2
  • Familial Pancreatic Cancer
  • FAMMM
  • Hereditary Pancreatitis
  • HNPCC
  • Lynch Syndrome
  • Pancreas Cancer
  • Pancreatic Adenocarcinoma
  • Pancreatic Cancer
  • Peutz Jeghers Syndrome
Design
Observational Model: OtherTime Perspective: Prospective

Participation Requirements

Age
Between 18 years and 125 years
Gender
Both males and females

Description

Interested individuals can be referred by physicians, or by family or friends. Individuals are informed that the purpose of this study is to collect outcome data following early detection testing based upon our criteria for elevated risk. Consent is obtained by any of the co-investigators. Consent i...

Interested individuals can be referred by physicians, or by family or friends. Individuals are informed that the purpose of this study is to collect outcome data following early detection testing based upon our criteria for elevated risk. Consent is obtained by any of the co-investigators. Consent is obtained for the primary PCEDP, and also obtained to allow for data to be used by our Cancer Program. We have a weekly review of all calls made and of all enrollments. We have a monthly meeting to review all proceeding regarding the study. Our IRB routinely reviews the proceedings of the study Our institution has a monthly Clinical research Committee meeting.

Tracking Information

NCT #
NCT02206360
Collaborators
Not Provided
Investigators
Not Provided