ID

15498

Beschrijving

Chemotherapy/Radiotherapy Versus Concomitant Chemotherapy Followed by Radiotherapy in Stage IIIB Non-small Cell Lung Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT01652820

Link

https://clinicaltrials.gov/show/NCT01652820

Trefwoorden

  1. 01-06-16 01-06-16 -
Geüploaded op

1 juni 2016

DOI

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Licentie

Creative Commons BY 4.0

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Eligibility Non Small-cell Lung Cancer NCT01652820

Eligibility Non Small-cell Lung Cancer NCT01652820

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
unresectable stage iiia or b nsclc patients
Beschrijving

nsclc

Datatype

boolean

Alias
UMLS CUI [1]
C0007131
who ps 0 or 1
Beschrijving

who ps

Datatype

boolean

Alias
UMLS CUI [1]
C1298650
weight loss < 5 % within the last 3 months
Beschrijving

weight loss

Datatype

boolean

Alias
UMLS CUI [1]
C1262477
at least one measurable lesion
Beschrijving

measurable lesion

Datatype

boolean

Alias
UMLS CUI [1]
C1513041
planning ct scan previous to randomization
Beschrijving

ct scan

Datatype

boolean

Alias
UMLS CUI [1]
C0040405
written informed consent
Beschrijving

written informed consent

Datatype

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
malignant effusion, supraclavicular node or svcs
Beschrijving

malignant effusion, supraclavicular node or svcs

Datatype

boolean

Alias
UMLS CUI [1]
C0080032
UMLS CUI [2]
C0229730
ptv > 2000 cm3
Beschrijving

ptv

Datatype

boolean

Alias
UMLS CUI [1]
C0454199
v20 > 35%
Beschrijving

v20

Datatype

boolean

fev1 and dlco both < 30% or 1 liter at study entry
Beschrijving

fev1 and dlco

Datatype

boolean

Alias
UMLS CUI [1]
C0748133
UMLS CUI [2]
C1516251

Similar models

Eligibility Non Small-cell Lung Cancer NCT01652820

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
nsclc
Item
unresectable stage iiia or b nsclc patients
boolean
C0007131 (UMLS CUI [1])
who ps
Item
who ps 0 or 1
boolean
C1298650 (UMLS CUI [1])
weight loss
Item
weight loss < 5 % within the last 3 months
boolean
C1262477 (UMLS CUI [1])
measurable lesion
Item
at least one measurable lesion
boolean
C1513041 (UMLS CUI [1])
ct scan
Item
planning ct scan previous to randomization
boolean
C0040405 (UMLS CUI [1])
written informed consent
Item
written informed consent
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
malignant effusion, supraclavicular node or svcs
Item
malignant effusion, supraclavicular node or svcs
boolean
C0080032 (UMLS CUI [1])
C0229730 (UMLS CUI [2])
ptv
Item
ptv > 2000 cm3
boolean
C0454199 (UMLS CUI [1])
v20
Item
v20 > 35%
boolean
fev1 and dlco
Item
fev1 and dlco both < 30% or 1 liter at study entry
boolean
C0748133 (UMLS CUI [1])
C1516251 (UMLS CUI [2])

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