Study centre number
Item
Site #
integer
C0600091 (UMLS CUI [1,1])
C0019994 (UMLS CUI [1,2])
patient ID
Item
Patient #
integer
C2348585 (UMLS CUI [1])
visit date
Item
Visit Date
date
C1320303 (UMLS CUI [1])
Investigator Name
Item
Investigator Name
text
C2826892 (UMLS CUI [1])
Additional form
Item
Check if additional supplemental instance of this form was used.
boolean
C1706499 (UMLS CUI [1])
CRF Sequential Number
Item
Instance Number
integer
C1516308 (UMLS CUI [1,1])
C2348184 (UMLS CUI [1,2])
Item
Assay
integer
C0332307 (UMLS CUI [1,1])
C0522876 (UMLS CUI [1,2])
CL Item
Other (Indicate and specify in Comments) (4)
Comments
Item
Comments
text
C0947611 (UMLS CUI [1])
Date of HIT assay
Item
Date
date
C0011008 (UMLS CUI [1,1])
C0522876 (UMLS CUI [1,2])
Item
Assay Results
text
C0522876 (UMLS CUI [1,1])
C1274040 (UMLS CUI [1,2])
CL Item
Positive (Positive)
CL Item
Negative (Negative)