ID

17652

Beskrivning

Sponsor: OSI Pharmaceuticals Information provided by (Responsible Party): Astellas Pharma Inc (OSI Pharmaceuticals) A multicenter, randomized, double-blind, placebo-controlled, phase 3 study of single-agent Tarceva® (erlotinib) following complete tumor resection with or without adjuvant chemotherapy in patients with stage IB-IIIA non-small cell lung carcinoma who have EGFR-positive tumors. See https://clinicaltrials.gov/ct2/show/NCT00373425 Part of study: Baseline Local Laboratory Data

Länk

https://clinicaltrials.gov/ct2/show/NCT00373425

Nyckelord

Versioner (4)
  1. 2016-08-01 2016-08-01 -
  2. 2016-09-27 2016-09-27 -
  3. 2022-04-01 2022-04-01 - Martin Dugas
  4. 2022-04-01 2022-04-01 - Martin Dugas
Uppladdad den

27 september 2016

DOI

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Licens

Creative Commons BY 4.0
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Baseline Local Laboratory Data, Tarceva in NSCLC patients who have EGFR-positive tumors DRKS00001485 NCT00373425

Engelsk

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

1 Formulär  
Hematology
Beskrivning

Hematology

Date
Beskrivning

Date

Datatyp

date

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

For each different lab, provide normal ranges.

Datatyp

text

Alias
UMLS CUI [1]
C1882331
Hemoglobin
Beskrivning

Hemoglobin

Datatyp

text

Alias
UMLS CUI [1]
C0518015
WBC
Beskrivning

WBC

Datatyp

text

Alias
UMLS CUI [1]
C0023508
ANC
Beskrivning

Neutrophil count

Datatyp

text

Alias
UMLS CUI [1]
C0200633
Platelet Count
Beskrivning

Platelet Count

Datatyp

text

Alias
UMLS CUI [1]
C0032181
Biochemistry
Beskrivning

Biochemistry

Date
Beskrivning

Date

Datatyp

date

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

For each different lab, provide normal ranges.

Datatyp

text

Alias
UMLS CUI [1]
C1882331
Creatinine
Beskrivning

Creatinine

Datatyp

text

Alias
UMLS CUI [1]
C0201976
Total Bilirubin
Beskrivning

Total Bilirubin

Datatyp

text

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

ALT

Datatyp

text

Alias
UMLS CUI [1]
C0201836
Sodium
Beskrivning

Sodium

Datatyp

text

Alias
UMLS CUI [1]
C0337443
Potassium
Beskrivning

Potassium

Datatyp

text

Alias
UMLS CUI [1]
C0202194
Magnesium
Beskrivning

Magnesium

Datatyp

text

Alias
UMLS CUI [1]
C0373675
Pregnancy Tests
Beskrivning

Pregnancy Tests

Pregnancy Test: Not Applicable
Beskrivning

Pregnancy Test

Datatyp

boolean

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

Pregnancy Tests

Datatyp

boolean

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

Pregnancy test date

Datatyp

date

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

If positive, complete an Initial Pregnancy Report form.

Datatyp

integer

Alias
UMLS CUI [1]
C0427777
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Similar models

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

1 Formulär
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
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: Not 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)
Tillbaka till toppen 

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