Spots Global Cancer Trial Database for Molecular Screening for Lynch Syndrome in Denmark
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Trial Identification
Brief Title: Molecular Screening for Lynch Syndrome in Denmark
Official Title: Molecular Screening for Lynch Syndrome in Denmark
Study ID: NCT01845753
Interventions
Study Description
Brief Summary: A clinically applicably strategy for molecular screening for Lynch Syndrome is being implemented in Denmark. Based on sequential analysis with immunohistochemistry and methylation analysis, patients with possible hereditary colorectal cancer are identified. These patients are offered genetic risk assessment and counselling. The study hypothesis is that molecular screening will identify more patients with Lynch Syndrome than the family history alone. Prospective data collection is performed using established clinical databases.
Detailed Description:
Keywords
Eligibility
Minimum Age:
Eligible Ages: CHILD, ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
Locations
Department of Pathology, Aalborg, , Denmark
Department of Clinical Genetics, Aarhus, , Denmark
Department of Pathology, Aarhus, , Denmark
Department of Pathology, Esbjerg, , Denmark
Department of Pathology, Hjørring, , Denmark
Department of Clinical Genetics, Odense, , Denmark
Department of Pathology, Odense, , Denmark
Department of Pathology, Sønderborg, , Denmark
Vejle Hospital, Vejle, , Denmark
Department of Clinical Genetics, Vejle, , Denmark
Department of Pathology, Vejle, , Denmark
Contact Details
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