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Baseline Local Laboratory Data, Tarceva in NSCLC patients who have EGFR-positive tumors NCT00373425

1 forms  
Hematology
Description

Hematology

Date
Description

Date

Data type

date

Alias
UMLS CUI [1,1]
C0022885
UMLS CUI [1,2]
C0011008
Lab Name
Description

For each different lab, provide normal ranges.

Data type

text

Alias
UMLS CUI [1]
C1882331
Hemoglobin
Description

Hemoglobin

Data type

text

Alias
UMLS CUI [1]
C0518015
WBC
Description

WBC

Data type

text

Alias
UMLS CUI [1]
C0023508
ANC
Description

Neutrophil count

Data type

text

Alias
UMLS CUI [1]
C0200633
Platelet Count
Description

Platelet Count

Data type

text

Alias
UMLS CUI [1]
C0032181
Biochemistry
Description

Biochemistry

Date
Description

Date

Data type

date

Alias
UMLS CUI [1,1]
C0022885
UMLS CUI [1,2]
C0011008
Lab Name
Description

For each different lab, provide normal ranges.

Data type

text

Alias
UMLS CUI [1]
C1882331
Creatinine
Description

Creatinine

Data type

text

Alias
UMLS CUI [1]
C0201976
Total Bilirubin
Description

Total Bilirubin

Data type

text

Alias
UMLS CUI [1]
C0201913
ALT (SGPT)
Description

ALT

Data type

text

Alias
UMLS CUI [1]
C0201836
Sodium
Description

Sodium

Data type

text

Alias
UMLS CUI [1]
C0337443
Potassium
Description

Potassium

Data type

text

Alias
UMLS CUI [1]
C0202194
Magnesium
Description

Magnesium

Data type

text

Alias
UMLS CUI [1]
C0373675
Pregnancy Tests
Description

Pregnancy Tests

Pregnancy Test: Applicable?
Description

Pregnancy Test

Data type

boolean

Alias
UMLS CUI [1]
C0032976
Was a serum pregnancy test performed?
Description

Pregnancy Tests

Data type

boolean

Alias
UMLS CUI [1]
C0032976
If Yes, date test performed:
Description

Pregnancy test date

Data type

date

Alias
UMLS CUI [1,1]
C0032976
UMLS CUI [1,2]
C0011008
Pregnancy test result
Description

If positive, complete an Initial Pregnancy Report form.

Data type

integer

Alias
UMLS CUI [1]
C0427777
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Baseline Local Laboratory Data, Tarceva in NSCLC patients who have EGFR-positive tumors NCT00373425

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Hematology
Date
Item
Date
date
C0022885 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
Laboratory Name
Item
Lab Name
text
C1882331 (UMLS CUI [1])
Hemoglobin
Item
Hemoglobin
text
C0518015 (UMLS CUI [1])
WBC
Item
WBC
text
C0023508 (UMLS CUI [1])
Neutrophil count
Item
ANC
text
C0200633 (UMLS CUI [1])
Platelet Count
Item
Platelet Count
text
C0032181 (UMLS CUI [1])
Item Group
Biochemistry
Date
Item
Date
date
C0022885 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
Laboratory Name
Item
Lab Name
text
C1882331 (UMLS CUI [1])
Creatinine
Item
Creatinine
text
C0201976 (UMLS CUI [1])
Total Bilirubin
Item
Total Bilirubin
text
C0201913 (UMLS CUI [1])
ALT
Item
ALT (SGPT)
text
C0201836 (UMLS CUI [1])
Sodium
Item
Sodium
text
C0337443 (UMLS CUI [1])
Potassium
Item
Potassium
text
C0202194 (UMLS CUI [1])
Magnesium
Item
Magnesium
text
C0373675 (UMLS CUI [1])
Item Group
Pregnancy Tests
Pregnancy Test
Item
Pregnancy Test: Applicable?
boolean
C0032976 (UMLS CUI [1])
Pregnancy Tests
Item
Was a serum pregnancy test performed?
boolean
C0032976 (UMLS CUI [1])
Pregnancy test date
Item
If Yes, date test performed:
date
C0032976 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
Item
Pregnancy test result
integer
C0427777 (UMLS CUI [1])
Pregnancy test method
Code List
Pregnancy test result
CL Item
Positive (1)
CL Item
Negative (2)
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