Date of subject completion or withdrawal
Item
Date of subject completion or withdrawal
date
C2983670 (UMLS CUI [1])
Item
Was the subject withdrawn from the study?
text
C0422727 (UMLS CUI [1])
Code List
Was the subject withdrawn from the study?
Item
If the subject was withdrawn from the study, complete the primary reason:
text
C0422727 (UMLS CUI [1,1])
C0392360 (UMLS CUI [1,2])
Code List
If the subject was withdrawn from the study, complete the primary reason:
CL Item
Adverse Event (Adverse Event)
CL Item
Protocol deviation (Protocol deviation)
CL Item
Subject reached protocol defined stopping criteria (Subject reached protocol defined stopping criteria)
CL Item
Study closed/terminated (Study closed/terminated)
CL Item
Lost to Follow-up (Lost to Follow-up)
CL Item
Investigator discretion, specify (Investigator discretion, specify)
CL Item
Withdrew consent (Withdrew consent)
Withdrawal from the study at the investigator's discretion, specification
Item
If you ticked 'Investigator discretion' as primary reason for withdrawal, specify
text
C2349954 (UMLS CUI [1,1])
C1710220 (UMLS CUI [1,2])
C0679006 (UMLS CUI [1,3])
C2348235 (UMLS CUI [1,4])
Item
Did a female partner of the male subject become pregnant during the study?
text
C0919624 (UMLS CUI [1])
Code List
Did a female partner of the male subject become pregnant during the study?
CL Item
Not applicable (Not applicable)
Item
Did the subject become pregnant during the study?
text
C0032961 (UMLS CUI [1])
Code List
Did the subject become pregnant during the study?