Study Coordinating Center, Identification number
Item
Centre Number
integer
C2825181 (UMLS CUI [1,1])
C1300638 (UMLS CUI [1,2])
Clinical Trial Subject Unique Identifier
Item
Patient Number
integer
C2348585 (UMLS CUI [1])
Person Initials
Item
Patient Initials
text
C2986440 (UMLS CUI [1])
Date of visit
Item
Visit Date
date
C1320303 (UMLS CUI [1])
Item
Relative Time
text
C1827287 (UMLS CUI [1,1])
C0439564 (UMLS CUI [1,2])
CL Item
Pre-Dose Reading 1 (1)
CL Item
Pre-Dose Reading 2 (2)
CL Item
Pre-Dose Reading 3 (3)
CL Item
2 hours Post-Dose Reading 1 (5)
Semi-erect; Vital Signs Time
Item
After 10 minutes semi-supine - Time Vitals Taken
time
C0522019 (UMLS CUI [1,1])
C2826762 (UMLS CUI [1,2])
Semi-erect; Systolic Pressure
Item
After 10 minutes semi-supine - Blood Pressure (systolic)
integer
C0522019 (UMLS CUI [1,1])
C0871470 (UMLS CUI [1,2])
Semi-erect; Diastolic blood pressure
Item
After 10 minutes semi-supine - Blood Pressure (diastolic)
integer
C0522019 (UMLS CUI [1,1])
C0428883 (UMLS CUI [1,2])
Semi-erect; Heart rate
Item
After 10 minutes semi-supine - Pulse
integer
C0522019 (UMLS CUI [1,1])
C0018810 (UMLS CUI [1,2])
Erect, Vital Signs Time
Item
After erect for 1 minute - Time Vitals Taken
time
C0522014 (UMLS CUI [1,1])
C2826762 (UMLS CUI [1,2])
Erect, Systolic Pressure
Item
After erect for 1 minute - Blood Pressure (systolic)
integer
C0522014 (UMLS CUI [1,1])
C0871470 (UMLS CUI [1,2])
Erect, Diastolic blood pressure
Item
After erect for 1 minute - Blood Pressure (diastolic)
integer
C0522014 (UMLS CUI [1,1])
C0428883 (UMLS CUI [1,2])
Erect, Heart rate
Item
After erect for 1 minute - Pulse
integer
C0522014 (UMLS CUI [1,1])
C0018810 (UMLS CUI [1,2])