Study End Date
Item
Date of end of study
date
C2983670 (UMLS CUI [1])
Item
Who ended the study?
integer
C2826892 (UMLS CUI [1,1])
C2732579 (UMLS CUI [1,2])
Code List
Who ended the study?
Premature end of study
Item
Premature end of study
boolean
C1279919 (UMLS CUI [1,1])
C2732579 (UMLS CUI [1,2])
Item
If Yes: reasons for discontinuation of the study (multiple reasons are possible)
integer
C0566251 (UMLS CUI [1,1])
C0457454 (UMLS CUI [1,2])
Code List
If Yes: reasons for discontinuation of the study (multiple reasons are possible)
CL Item
lost to follow up (1)
CL Item
Withdrawal of consent (3)
CL Item
non-compliance of the patient (4)
CL Item
forbidden concomitant therapy (5)
CL Item
disease progression (6)
CL Item
adverse events (7)
Reason for discontination: Specification
Item
Other:
text
C0566251 (UMLS CUI [1,1])
C0457454 (UMLS CUI [1,2])
C2348235 (UMLS CUI [1,3])
Remarks or events
Item
Other remarks or events
text
C0947611 (UMLS CUI [1])
C0441471 (UMLS CUI [2])
Investigator's name
Item
Investigator's name
text
C2826892 (UMLS CUI [1])
Investigator's stamp
Item
Investigator's stamp
boolean
C3825804 (UMLS CUI [1])