Subject ID
Item
Subject ID
text
C2348585 (UMLS CUI [1])
Site Number
Item
Site No
text
C0018704 (UMLS CUI [1,1])
C0600091 (UMLS CUI [1,2])
Screening number
Item
Screening no
text
C1710477 (UMLS CUI [1])
Informed consent availability
Item
Signed and dated informed consent of the patient is available before start of any trial specific procedures
boolean
C0021430 (UMLS CUI [1,1])
C0470187 (UMLS CUI [1,2])
Date of informed consent
Item
Date of informed consent
date
C2985782 (UMLS CUI [1])
Study subject participation status
Item
Participation in contributing scientific investigations
boolean
C2348568 (UMLS CUI [1])