Status:
COMPLETED
Sequencing to Identify Gene Variants in Familial Colorectal Cancer
Lead Sponsor:
Norwegian University of Science and Technology
Collaborating Sponsors:
St. Olavs Hospital
Conditions:
Colorectal Cancer
Eligibility:
All Genders
20+ years
Brief Summary
The project will use exome sequencing to search for genetic predispositions for familial colorectal cancer (CRC). Except for certain syndromes there is today no good method for identifying individuals...
Detailed Description
Participants will be from a specific family, and will be selected by invitation to volunteer.
Eligibility Criteria
Inclusion
- Member of a specific family with increased risk of CRC, including individuals both with and without CRC
Exclusion
- Young age
Key Trial Info
Start Date :
December 1 2012
Trial Type :
OBSERVATIONAL
Allocation :
ACTUAL
End Date :
June 1 2016
Estimated Enrollment :
14 Patients enrolled
Trial Details
Trial ID
NCT01904630
Start Date
December 1 2012
End Date
June 1 2016
Last Update
July 14 2016
Active Locations (1)
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1
St Olavs Hospital
Trondheim, Norway