The GEOLynch Cohort Study
Recruiting now
Conditions studied: Lynch Syndrome, Neoplasms, Hereditary Nonpolyposis Colorectal Cancer, Colorectal Neoplasms
In brief
The GEOLynch cohort study has been established to investigate the influence of genetic, environmental and other factors on tumour risk in persons with Lynch syndrome.
Key facts
- Study ID
- NCT03303833
- Run by
- Wageningen University
- People needed
- 1000
- Starts
- 2006-07-01
- Expected to finish
- 2030-12-01
- Last updated by the study team
- 2017-10-06
Who can join
Age: 18 and older, up to 80. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Persons with a known mutation in a gene that causes Lynch syndrome, i.e. with an inherited monoallelic pathogenic germline mutation in either the MLH1, MSH2, MSH6, PMS2 or EPCAM gene.
- Aged between 18 and 80 years at inclusion.
You may not qualify if…
- Additional carrier of another hereditary colon cancer predisposition syndrome (e.g. FAP)
- (Chronic) Inflammatory bowel disease
- Non-Dutch speaking
- Dementia or another mental condition that makes it impossible to fill out questionnaires
- Terminally ill persons
Where it is running
- Wageningen University — Wageningen, Netherlands (enrolling)
Full record on ClinicalTrials.gov
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