NCT01904630View on ClinicalTrials.gov

Sequencing to Identify Gene Variants in Familial Colorectal Cancer

CompletedOBSERVATIONAL
Enrollment

14

Participants

Timeline

Start Date

December 31, 2012

Primary Completion Date

June 30, 2016

Study Completion Date

June 30, 2016

Conditions
Colorectal Cancer
Interventions
GENETIC

gene sequencing

Gene sequencing by exome capture and high throughput sequencing for identification of rare variants

Trial Locations (1)

Unknown

St Olavs Hospital, Trondheim

All Listed Sponsors
collaborator

St. Olavs Hospital

OTHER

lead

Norwegian University of Science and Technology

OTHER

NCT01904630 - Sequencing to Identify Gene Variants in Familial Colorectal Cancer | Biotech Hunter | Biotech Hunter