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])
Additional form
Item
Check if (additional) supplemental instance of this form was used.
boolean
C1706499 (UMLS CUI [1])
CRF Sequential Number
Item
Instance Number
integer
C1516308 (UMLS CUI [1,1])
C2348184 (UMLS CUI [1,2])
Transfusion during clinical trial
Item
Was a transfusion given during the Argatroban treatment period?
boolean
C1879316 (UMLS CUI [1,1])
C0347984 (UMLS CUI [1,2])
C0008976 (UMLS CUI [1,3])
Item
Blood Component Code
integer
C0005841 (UMLS CUI [1,1])
C1705248 (UMLS CUI [1,2])
Code List
Blood Component Code
CL Item
Cryoprecipitate (2)
CL Item
Autotransfusion (6)
CL Item
Other (specify under Reason for Transfusion) (7)
Transfusion start date
Item
Transfusion Start Date
date
C1879316 (UMLS CUI [1,1])
C0808070 (UMLS CUI [1,2])
Transfusion start time
Item
Start Time
time
C1879316 (UMLS CUI [1,1])
C1301880 (UMLS CUI [1,2])
Transfusion stop date
Item
Transfusion Stop Date
date
C1879316 (UMLS CUI [1,1])
C0806020 (UMLS CUI [1,2])
Transfusion stop time
Item
Stop Time
text
C1879316 (UMLS CUI [1,1])
C1522314 (UMLS CUI [1,2])
Quantity of transfusion
Item
# of units or cc transfused
integer
C1879316 (UMLS CUI [1,1])
C1265611 (UMLS CUI [1,2])
Item
Units or cc
text
C1519795 (UMLS CUI [1,1])
C1879316 (UMLS CUI [1,2])
C1265611 (UMLS CUI [1,3])
Reason for transfusion
Item
Reason for Transfusion
text
C0392360 (UMLS CUI [1,1])
C1879316 (UMLS CUI [1,2])