Center
Item
Center
text
C1301943 (UMLS CUI [1,1])
C0600091 (UMLS CUI [1,2])
Subject ID
Item
Subject ID
text
C2348585 (UMLS CUI [1])
Initials
Item
Initials
text
C2986440 (UMLS CUI [1])
Visit Date
Item
Visit Date
date
C1320303 (UMLS CUI [1])
Investigational Product Container Number
Item
Investigational Product Container Number
text
C0304229 (UMLS CUI [1,1])
C0180098 (UMLS CUI [1,2])
C0600091 (UMLS CUI [1,3])
Item
Investigational Product Type
integer
C0304229 (UMLS CUI [1,1])
C0332307 (UMLS CUI [1,2])
Code List
Investigational Product Type
CL Item
Double-blind tablets (1)
CL Item
Single-blind tablets (2)
Item
Blinded Dose Level
integer
C3174092 (UMLS CUI [1,1])
C0304229 (UMLS CUI [1,2])
C0013072 (UMLS CUI [1,3])
Code List
Blinded Dose Level
Start Date Investigational Product
Item
Start Date Investigational Product
date
C0304229 (UMLS CUI [1,1])
C0808070 (UMLS CUI [1,2])
Stop Date Investigational Product
Item
Stop Date Investigational Product
date
C0304229 (UMLS CUI [1,1])
C0806020 (UMLS CUI [1,2])