Date last contact
Item
Date of last contact
date
C0805839 (UMLS CUI [1])
Patient withdrawn from trial
Item
Was the subject withdrawn from the study?
boolean
C0422727 (UMLS CUI [1])
Patient withdrawn from trial; Decision; Date in time
Item
If subject was withdrawn from the study, date of decision to withdraw
date
C0422727 (UMLS CUI [1,1])
C0679006 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
Item
If subject was withdrawn from study, reason for withdrawal
integer
C0422727 (UMLS CUI [1,1])
C0392360 (UMLS CUI [1,2])
Code List
If subject was withdrawn from study, reason for withdrawal
CL Item
Adverse Event (Record details on the Non- Serious Adverse Events or Serious Adverse Events forms as appropriate) (1)
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 (Select this reason if none of the other primary reasons are appropriate) (7)
CL Item
Withdrew consent (8)
Patient withdrawn from trial; Indication; Clinical Investigators; Specification
Item
If primary reason for withdrawal is investigator discretion, please specify.
text
C0422727 (UMLS CUI [1,1])
C3146298 (UMLS CUI [1,2])
C0008961 (UMLS CUI [1,3])
C2348235 (UMLS CUI [1,4])