Study centre number
Item
Site #
integer
C0600091 (UMLS CUI [1,1])
C0019994 (UMLS CUI [1,2])
patient ID
Item
Patient #
integer
C2348585 (UMLS CUI [1])
visit date
Item
Visit Date
date
C1320303 (UMLS CUI [1])
Investigator Name
Item
Investigator Name
text
C2826892 (UMLS CUI [1])
Item
Is patient a neonate with a corrected gestational age of <44 weeks at enrollment?
text
C0021289 (UMLS CUI [1,1])
C3831006 (UMLS CUI [1,2])
Code List
Is patient a neonate with a corrected gestational age of <44 weeks at enrollment?
Item
Timepoint of Head Ultrasonography
text
C2348792 (UMLS CUI [1,1])
C0041618 (UMLS CUI [1,2])
C0018670 (UMLS CUI [1,3])
Code List
Timepoint of Head Ultrasonography
CL Item
Baseline Ultrasound (Baseline Ultrasound)
CL Item
Therapeutically Anticoagulated (Therapeutically Anticoagulated)
CL Item
Post-Treatment or 30-day Follow-Up (Post-Treatment or 30-day Follow-Up)
Head ultrasonography not done
Item
Not done
boolean
C0041618 (UMLS CUI [1,1])
C0018670 (UMLS CUI [1,2])
C1272696 (UMLS CUI [1,3])
Head ultrasonography date
Item
Date Performed
date
C0041618 (UMLS CUI [1,1])
C0018670 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
Head ultrasonography time
Item
Time Performed
time
C0041618 (UMLS CUI [1,1])
C0018670 (UMLS CUI [1,2])
C0040223 (UMLS CUI [1,3])
Item
Results
text
C0041618 (UMLS CUI [1,1])
C0018670 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
CL Item
Positive (bleeding, Grade 1 or above) (Positive (bleeding, Grade 1 or above))
CL Item
Negative (Negative)