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])
Date of beta-HCG test
Item
Date:
date
C0011008 (UMLS CUI [1,1])
C1255526 (UMLS CUI [1,2])
Time of beta-HCG test
Item
Time:
time
C0040223 (UMLS CUI [1,1])
C1255526 (UMLS CUI [1,2])
Beta-HCG test not performed
Item
Not Done
boolean
C1255526 (UMLS CUI [1,1])
C0445106 (UMLS CUI [1,2])
Beta-HCG test not applicable
Item
Not Applicable
boolean
C1255526 (UMLS CUI [1,1])
C1272460 (UMLS CUI [1,2])
Item
Results:
text
C1255526 (UMLS CUI [1,1])
C1274040 (UMLS CUI [1,2])
CL Item
Negative (Negative)
CL Item
Positive (Patient is to be excluded) (Positive (Patient is to be excluded))