C18 C19 C20
Conditions
Interventions
Group 1: Observational Study with diagnostic intervention: the participants will be asked to donate a blood sample, 2 native stool samples and to perform 2 FIT and one Hemoccult test.
Sponsors
Deutsches Krebsforschungszentrum Heidelberg
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: participants in screening colonoscopy, informed consent
Exclusion criteria
Exclusion criteria: Inadequate knowledge of German, diagnostic colonoscopy, missing informed consent document
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| sensitivity and specificity of tests for the detection of advanced colorectal neoplasia | — |
Secondary
| Measure | Time frame |
|---|---|
| sensitivity and specificity of tests for the detection of colorectal carcinomas, advanced colorectal adenomas and other colorectal adenomas | — |
Countries
Germany
Contacts
Public ContactJason Hochhaus
Deutsches Krebsforschungszentrum Heidelberg
Outcome results
None listed