Subject Number
Item
Subject Number
text
C2348585 (UMLS CUI [1])
Study Conclusion
Item
Did the subject complete the study as planned?
boolean
C1707478 (UMLS CUI [1,1])
C0008972 (UMLS CUI [1,2])
Item
If ’NO’, mark the one most appropriate category
integer
C1707478 (UMLS CUI [1,1])
C0008972 (UMLS CUI [1,2])
Code List
If ’NO’, mark the one most appropriate category
CL Item
Adverse Event (complete Adverse Event Form) (1)
C0877248 (UMLS CUI-1)
(Comment:en)
CL Item
Insufficient therapeutic effect (2)
C1527144 (UMLS CUI-1)
(Comment:en)
CL Item
Deviation from Protocol (including non-compliance) (3)
C1321605 (UMLS CUI-1)
(Comment:en)
CL Item
Lost to Follow-Up (4)
C1302313 (UMLS CUI-1)
(Comment:en)
CL Item
Other (5)
C0205394 (UMLS CUI-1)
(Comment:en)
Other
Item
Other, Please specify
text
C0205394 (UMLS CUI [1])
Comment reason for withdrawal
Item
Comments on reason for withdrawal:
text
C0947611 (UMLS CUI [1,1])
C2349954 (UMLS CUI [1,2])
C0392360 (UMLS CUI [1,3])
C0008976 (UMLS CUI [1,4])
Date of Withdrawal
Item
Date of Withdrawal:
date
C2349954 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
Time of Withdrawal
Item
Time of Withdrawal:
time
C2349954 (UMLS CUI [1,1])
C0040223 (UMLS CUI [1,2])
Date of Final Dose
Item
Date of Final Dose:
date
C1531784 (UMLS CUI [1])
Time of Final Dose
Item
Time of Final Dose:
time
C0946444 (UMLS CUI [1])