Patient Study ID
Item
Patient ID
text
C2348585 (UMLS CUI [1])
Verification of eligibility criteria
Item
Are all inclusion criteria met?
boolean
C1516637 (UMLS CUI [1,1])
C1711411 (UMLS CUI [1,2])
Verification of eligibility criteria
Item
Have any exclusion criteria been answered with yes?
boolean
C1516637 (UMLS CUI [1,1])
C1711411 (UMLS CUI [1,2])
Informed consent
Item
Informed consent signed
boolean
C0021430 (UMLS CUI [1])
Date of informed consent
Item
Date of informed consent
date
C0011008 (UMLS CUI [1,1])
C0021430 (UMLS CUI [1,2])
Study site
Item
Study site number
integer
C2825164 (UMLS CUI [1])
Item
Age
text
C0001779 (UMLS CUI [1])
Item
Gender
integer
C0079399 (UMLS CUI [1])
Item
Modified rankin scale score
text
C2984908 (UMLS CUI [1])
Code List
Modified rankin scale score
Phone contact
Item
Please enter a phone number for further questions that might occur
integer
C3476398 (UMLS CUI [1])
Fax number
Item
Please enter a valid fax number
integer
C1549619 (UMLS CUI [1])
Date of Randomization
Item
Date of Randomization
date
C0034656 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
Signature
Item
Signature by investigator
text
C1519316 (UMLS CUI [1])
Name of Investigator
Item
Name of Investigator
text
C0008961 (UMLS CUI [1])
Item
Patient has been randomized into following group
text
C0034656 (UMLS CUI [1])
Code List
Patient has been randomized into following group
CL Item
CABG with CEA (1)
CL Item
CABG without CEA (2)
Date of Randomization
Item
Date of Randomization
date
C0034656 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
Signature
Item
Signature by randomizing Person
text
C1519316 (UMLS CUI [1])
Name
Item
Name of randomizing person
text
C0027365 (UMLS CUI [1])