Date of Visit/ Assessment
Item
Date of Visit/ Assessment
date
C1320303 (UMLS CUI [1,1])
C2985720 (UMLS CUI [1,2])
Is the subject continuing in the study?
Item
Is the subject continuing in the study?
boolean
C0805733 (UMLS CUI [1])
Did the subject fail to complete this phase of the study?
Item
Did the subject fail to complete this phase of the study?
boolean
C0805732 (UMLS CUI [1,1])
C0231175 (UMLS CUI [1,2])
C0205390 (UMLS CUI [2,1])
C2603343 (UMLS CUI [2,2])
Date subject failed to complete
Item
Date subject failed to complete
date
C0805732 (UMLS CUI [1,1])
C0231175 (UMLS CUI [1,2])
C0205390 (UMLS CUI [2,1])
C2603343 (UMLS CUI [2,2])
C0011008 (UMLS CUI [3])
Item
Primary reason for withdrawal
integer
C0422727 (UMLS CUI [1,1])
C0392360 (UMLS CUI [1,2])
Code List
Primary reason for withdrawal
CL Item
Adverse event (1)
CL Item
Lack of efficacy (2)
CL Item
Protocol deviation (3)
CL Item
Subject reached protocol-defined stopping criteria (4)
CL Item
Study closed/terminated (5)
CL Item
Lost to follow-up (6)
CL Item
Investigator discretion, specify (7)
CL Item
Withdrew consent, specify (8)
CL Item
Prohibited medication use (029)
Specify Investigator discretion
Item
Specify Investigator discretion
text
C2348235 (UMLS CUI [1,1])
C0008961 (UMLS CUI [1,2])
C0022423 (UMLS CUI [1,3])
Specify withdrew consent
Item
Specify withdrew consent
text
C1707492 (UMLS CUI [1,1])
C2348235 (UMLS CUI [1,2])