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])
Surgery or invasive procedure during clinical trial
Item
Did the patient undergo surgery or other invasive procedure during the study period?
boolean
C0543467 (UMLS CUI [1,1])
C0347984 (UMLS CUI [1,2])
C0008976 (UMLS CUI [1,3])
C4048276 (UMLS CUI [2,1])
C0347984 (UMLS CUI [2,2])
C0008976 (UMLS CUI [2,3])
Type of surgery/procedure
Item
Type of Surgery / Procedure
text
C0543467 (UMLS CUI [1,1])
C0455713 (UMLS CUI [1,2])
C4048276 (UMLS CUI [2,1])
C0455713 (UMLS CUI [2,2])
Date of surgery or invasive procedure
Item
Date
date
C0543467 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
C4048276 (UMLS CUI [2,1])
C0011008 (UMLS CUI [2,2])
Time of surgery or invasive procedure
Item
Time
time
C0543467 (UMLS CUI [1,1])
C0040223 (UMLS CUI [1,2])
C4048276 (UMLS CUI [2,1])
C0040223 (UMLS CUI [2,2])
Indication of surgery/invasive procedure
Item
Underlying Condition Necessitating Surgery / Procedure
text
C3146298 (UMLS CUI [1,1])
C0543467 (UMLS CUI [1,2])
C3146298 (UMLS CUI [2,1])
C4048276 (UMLS CUI [2,2])