LOCKED
Item
Locked
text
C3244297 (UMLS CUI [1, 1])
LAB
Item
Lab and lab range subset
text
C0022877 (UMLS CUI [1,1])
C0022877 (UMLS CUI [2,1])
C1514721 (UMLS CUI [2,2])
C1515021 (UMLS CUI [2,3])
QUALVAL
Item
Qualifying Value
text
C1514624,C1522609 (UMLS CUI [1, 1])
HEADCMT
Item
Header Comment
text
C0947611 (UMLS CUI [1, 1])
INV
Item
Investigator
text
C0035173 (UMLS CUI [1, 1])
SITE
Item
Site
text
C0205145 (UMLS CUI [1, 1])
SUBVISIT
Item
Subevent
text
C2983704 (UMLS CUI [1,1])
C0441471 (UMLS CUI [1,2])
VISIT
Item
Clinical Planned Event
text
C0205210 (UMLS CUI [1,1])
C0441471 (UMLS CUI [1,2])
C1301732 (UMLS CUI [1,3])
BLANK
Item
Blank Flag
text
C1708067 (UMLS CUI [1, 1])
DCMDATE
Item
DCM Date
date
C1302413 (UMLS CUI [1, 1])
DOCNUM
Item
Document Number
text
C2986015 (UMLS CUI [1, 1])
PATIENT
Item
Patient
text
C0030705 (UMLS CUI [1, 1])
Item
Primary reason for trial completion
text
C2732579 C1549995 (UMLS CUI [1, 1])
Code List
Primary reason for trial completion
CL Item
Patient completed (1)
CL Item
AE study dis. worse (2)
CL Item
AE oth. dis. worse (3)
CL Item
Non compl. protocol (5)
CL Item
Lost to follow-up (6)
CL Item
Consent withdrawn (7)
TERMX
Item
Explanation/Comment
text
C0947611 (UMLS CUI [1, 1])
Item
Informed Consent Given for Vital status
text
C0021430,C1148433 (UMLS CUI [1, 1])
Code List
Informed Consent Given for Vital status
CL Item
No (0)
C1298908 (UMLS CUI [1,1])
CL Item
Yes (1)
C1705108 (UMLS CUI [1,1])
ATRCD
Item
Actual Treatment Code
text
C0087111,C0805701 (UMLS CUI [1, 1])
ATRSTDT
Item
Actual Treatment Start Date
date
C3173309 (UMLS CUI [1, 1])
ATRSTTM
Item
Actual Treatment Start Time
partialTime
C0087111,C1301880 (UMLS CUI [1, 1])