Colorectal Carcinoma
Item
patients with verifies colorectal cancer (group 1)
boolean
C0009402 (UMLS CUI [1])
Gastric carcinoma
Item
patients with verified gastric cancer (group 5)
boolean
C0699791 (UMLS CUI [1])
Colonoscopy Due to Indication
Item
patients undergoing colonoscopy due to clinical indications (group 2-4)
boolean
C0009378 (UMLS CUI [1,1])
C0678226 (UMLS CUI [1,2])
C3146298 (UMLS CUI [1,3])
Upper endoscopy Due to Indication
Item
patients undergoing upper endoscopy due to clinical indications (group 6-8)
boolean
C0017195 (UMLS CUI [1,1])
C0678226 (UMLS CUI [1,2])
C3146298 (UMLS CUI [1,3])
Study Population group | Average Risk | Age | Symptom severe Absent
Item
average-risk population group aged 40-64 at inclusion without alarm symptoms (group 9)
boolean
C2348561 (UMLS CUI [1])
C1510992 (UMLS CUI [2,1])
C0035647 (UMLS CUI [2,2])
C0001779 (UMLS CUI [3])
C0436345 (UMLS CUI [4,1])
C0332197 (UMLS CUI [4,2])
Motivation Participation Clinical Trial
Item
motivation to participate in the study
boolean
C0026605 (UMLS CUI [1,1])
C0679823 (UMLS CUI [1,2])
C0008976 (UMLS CUI [1,3])
Patient physical state allowing Interventional procedure
Item
physical status allowing volatile marker sampling and other procedures within the protocol
boolean
C0679834 (UMLS CUI [1,1])
C0683607 (UMLS CUI [1,2])
C0184661 (UMLS CUI [1,3])
Informed Consent
Item
signed consent
boolean
C0021430 (UMLS CUI [1])
Cancer Other
Item
known other active cancer
boolean
C1707251 (UMLS CUI [1])
Respiration Disorders | Airway Obstruction
Item
ventilation problems, airway obstruction
boolean
C0035204 (UMLS CUI [1])
C0001883 (UMLS CUI [2])
Cooperation Unwilling | Cooperation Unable
Item
unwillingness or inability to co-operate
boolean
C0392337 (UMLS CUI [1,1])
C0558080 (UMLS CUI [1,2])
C0392337 (UMLS CUI [2,1])
C1299582 (UMLS CUI [2,2])