ID

34432

Description

Prognostic Value of Tumor Hypoxia, as Measured by 18F-FMISO Breath Hold PET/CT, in Non-Small-Cell-Lung Cancer (NSCLC) Patients; ODM derived from: https://clinicaltrials.gov/show/NCT02016872

Link

https://clinicaltrials.gov/show/NCT02016872

Keywords

  1. 1/17/19 1/17/19 -
Copyright Holder

see on clinicaltrials.gov

Uploaded on

January 17, 2019

DOI

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License

Creative Commons BY 4.0

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Eligibility Non-Small-Cell-Lung Cancer (NSCLC) NCT02016872

Eligibility Non-Small-Cell-Lung Cancer (NSCLC) NCT02016872

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
pathologic confirmation of nsclc at mskcc
Description

ID.1

Data type

boolean

no prior treatment for this diagnosis of nsclc
Description

ID.2

Data type

boolean

patient to be treated with neoadjuvant chemotherapy (35 patients total) or patient to be treated with definitive rt,sequential chemo-rt, or concurrent chemo-rt (minimum dose of 50 gy in 25 fractions) (25 patients total)
Description

ID.3

Data type

boolean

primary tumor or nodal tumor must measure ≥ 2 cm on ct (hilar and mediastinal ln excluded)
Description

ID.4

Data type

boolean

age ≥ 18 years
Description

ID.5

Data type

boolean

ability to hold the breath for 10 seconds.
Description

ID.6

Data type

boolean

karnofsky performance status ≥ 70%
Description

ID.7

Data type

boolean

women of childbearing age must have a negative blood pregnancy test
Description

ID.8

Data type

boolean

Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
women who are pregnant or breast-feeding
Description

ID.9

Data type

boolean

severe diabetes (fasting blood glucose > 200 mg/dl)
Description

ID.10

Data type

boolean

Similar models

Eligibility Non-Small-Cell-Lung Cancer (NSCLC) NCT02016872

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
pathologic confirmation of nsclc at mskcc
boolean
ID.2
Item
no prior treatment for this diagnosis of nsclc
boolean
ID.3
Item
patient to be treated with neoadjuvant chemotherapy (35 patients total) or patient to be treated with definitive rt,sequential chemo-rt, or concurrent chemo-rt (minimum dose of 50 gy in 25 fractions) (25 patients total)
boolean
ID.4
Item
primary tumor or nodal tumor must measure ≥ 2 cm on ct (hilar and mediastinal ln excluded)
boolean
ID.5
Item
age ≥ 18 years
boolean
ID.6
Item
ability to hold the breath for 10 seconds.
boolean
ID.7
Item
karnofsky performance status ≥ 70%
boolean
ID.8
Item
women of childbearing age must have a negative blood pregnancy test
boolean
Item Group
C0680251 (UMLS CUI)
ID.9
Item
women who are pregnant or breast-feeding
boolean
ID.10
Item
severe diabetes (fasting blood glucose > 200 mg/dl)
boolean

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