ID

16711

Descripción

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

Link

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

Palabras clave

Versiones (4)
  1. 1/8/16 1/8/16 -
  2. 27/9/16 27/9/16 -
  3. 1/4/22 1/4/22 - Martin Dugas
  4. 1/4/22 1/4/22 - Martin Dugas
Subido en

1 de agosto de 2016

DOI

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Licencia

Creative Commons BY-NC 3.0
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Baseline Local Laboratory Data, Tarceva in NSCLC patients who have EGFR-positive tumors NCT00373425

Inglés

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

1 formularios  
Hematology
Descripción

Hematology

Date
Descripción

Date

Tipo de datos

date

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

For each different lab, provide normal ranges.

Tipo de datos

text

Alias
UMLS CUI [1]
C1882331
Hemoglobin
Descripción

Hemoglobin

Tipo de datos

text

Alias
UMLS CUI [1]
C0518015
WBC
Descripción

WBC

Tipo de datos

text

Alias
UMLS CUI [1]
C0023508
ANC
Descripción

Neutrophil count

Tipo de datos

text

Alias
UMLS CUI [1]
C0200633
Platelet Count
Descripción

Platelet Count

Tipo de datos

text

Alias
UMLS CUI [1]
C0032181
Biochemistry
Descripción

Biochemistry

Date
Descripción

Date

Tipo de datos

date

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

For each different lab, provide normal ranges.

Tipo de datos

text

Alias
UMLS CUI [1]
C1882331
Creatinine
Descripción

Creatinine

Tipo de datos

text

Alias
UMLS CUI [1]
C0201976
Total Bilirubin
Descripción

Total Bilirubin

Tipo de datos

text

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

ALT

Tipo de datos

text

Alias
UMLS CUI [1]
C0201836
Sodium
Descripción

Sodium

Tipo de datos

text

Alias
UMLS CUI [1]
C0337443
Potassium
Descripción

Potassium

Tipo de datos

text

Alias
UMLS CUI [1]
C0202194
Magnesium
Descripción

Magnesium

Tipo de datos

text

Alias
UMLS CUI [1]
C0373675
Pregnancy Tests
Descripción

Pregnancy Tests

Pregnancy Test: Applicable?
Descripción

Pregnancy Test

Tipo de datos

boolean

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

Pregnancy Tests

Tipo de datos

boolean

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

Pregnancy test date

Tipo de datos

date

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

If positive, complete an Initial Pregnancy Report form.

Tipo de datos

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 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
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)
Volver a la parte superior de la página 

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