Institution name, Identifier
Item
Center Number
integer
C1301943 (UMLS CUI [1,1])
C0600091 (UMLS CUI [1,2])
Patient number
Item
Patient Number
integer
C1830427 (UMLS CUI [1])
Person Initials
Item
Patient Initials
text
C2986440 (UMLS CUI [1])
Clinical Research, Complete
Item
Did the patient complete the study as planned?
boolean
C0008972 (UMLS CUI [1,1])
C0205197 (UMLS CUI [1,2])
Item
If ’No’, mark the Primary cause of withdrawal
text
C0008972 (UMLS CUI [1,1])
C2349954 (UMLS CUI [1,2])
C3146298 (UMLS CUI [1,3])
Code List
If ’No’, mark the Primary cause of withdrawal
CL Item
Adverse Experience (1)
CL Item
Insufficient therapeutic effect (2)
CL Item
Protocol deviation (including non-compliance) (3)
CL Item
Lost to follow-up (4)
CL Item
Other - specify (5)
Clinical Research, Withdraw, Indication
Item
Specification / Comments on the reason for withdrawal
text
C0008972 (UMLS CUI [1,1])
C2349954 (UMLS CUI [1,2])
C3146298 (UMLS CUI [1,3])
Clinical Research, Assessment Date
Item
Date of Final Study Evaluation
date
C0008972 (UMLS CUI [1,1])
C2985720 (UMLS CUI [1,2])