ID

34432

Beskrivning

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

Länk

https://clinicaltrials.gov/show/NCT02016872

Nyckelord

  1. 2019-01-17 2019-01-17 -
Rättsinnehavare

see on clinicaltrials.gov

Uppladdad den

17 januari 2019

DOI

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Licens

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
Beskrivning

Inclusion Criteria

Alias
UMLS CUI
C1512693
pathologic confirmation of nsclc at mskcc
Beskrivning

ID.1

Datatyp

boolean

no prior treatment for this diagnosis of nsclc
Beskrivning

ID.2

Datatyp

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)
Beskrivning

ID.3

Datatyp

boolean

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

ID.4

Datatyp

boolean

age ≥ 18 years
Beskrivning

ID.5

Datatyp

boolean

ability to hold the breath for 10 seconds.
Beskrivning

ID.6

Datatyp

boolean

karnofsky performance status ≥ 70%
Beskrivning

ID.7

Datatyp

boolean

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

ID.8

Datatyp

boolean

Exclusion Criteria
Beskrivning

Exclusion Criteria

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

ID.9

Datatyp

boolean

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

ID.10

Datatyp

boolean

Similar models

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

Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
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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