ID

15614

Beskrivning

EF5 in Measuring Tumor Hypoxia in Patients With Stage I-III Non-Small Cell Lung Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT02154399

Länk

https://clinicaltrials.gov/show/NCT02154399

Nyckelord

  1. 2016-06-05 2016-06-05 -
Uppladdad den

5 juni 2016

DOI

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Licens

Creative Commons BY 4.0

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Eligibility Stage IA Non-Small Cell Lung Carcinoma NCT02154399

Eligibility Stage IA Non-Small Cell Lung Carcinoma NCT02154399

Inclusion Criteria
Beskrivning

Inclusion Criteria

Alias
UMLS CUI
C1512693
known or suspected non-small cell lung cancer; patients without histologically or cytologically documented non-small cell lung cancer (nsclc) must be estimated by their physician to have at least 75% probability of having nsclc; the probability of malignancy will be predicted on the basis of known probabilities of individual clinical characteristics using a bayesian model
Beskrivning

non-small cell lung cancer

Datatyp

boolean

Alias
UMLS CUI [1]
C0007131
clinical or pathologic stage i to iii; patients in whom pre-surgical staging has not definitively establish stage iv disease are eligible
Beskrivning

clinical or pathologic stage i to iii

Datatyp

boolean

Alias
UMLS CUI [1]
C0027646
tumor mass at least 1.5 cm in maximum diameter must be present on computed tomography (ct) scan and must be included in the planned surgical biopsy or resection
Beskrivning

tumor mass size

Datatyp

boolean

Alias
UMLS CUI [1,1]
C3273930
UMLS CUI [1,2]
C0205099
patient must be planning to undergo a surgical staging or treatment procedure (including mediastinoscopy, wedge resection, lobectomy, or pneumonectomy) and have the clinical and physiological status appropriate for this procedure
Beskrivning

surgical staging

Datatyp

boolean

Alias
UMLS CUI [1]
C0543467
performance status 0-2
Beskrivning

performance status

Datatyp

boolean

Alias
UMLS CUI [1]
C1520224
bilirubin within normal limits
Beskrivning

bilirubin

Datatyp

boolean

Alias
UMLS CUI [1]
C0005437
creatinine within normal limits or, if elevated, a creatinine clearance of at least 60 ml/min/m^2 (ef5 is primarily excreted via the kidney)
Beskrivning

creatinine

Datatyp

boolean

Alias
UMLS CUI [1]
C0010294
UMLS CUI [2]
C0373595
white blood cell (wbc) > 2000/mm^3
Beskrivning

WBC

Datatyp

boolean

Alias
UMLS CUI [1]
C0023508
platelets > 100,000/mm^3
Beskrivning

platelets

Datatyp

boolean

Alias
UMLS CUI [1]
C0005821
Exclusion Criteria
Beskrivning

Exclusion Criteria

Alias
UMLS CUI
C0680251
pregnancy or breast feeding; a negative serum pregnancy test is required of any woman of childbearing potential prior to enrollment; pregnant women are excluded from this study; breastfeeding should be discontinued if the mother is treated with ef5
Beskrivning

pregnancy or breast feeding

Datatyp

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
allergy to iv contrast dye
Beskrivning

allergy to iv contrast dye

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C0742795
history of grade iii or iv peripheral neuropathy as defined by the national cancer institute (nci) common terminology criteria (ctc)
Beskrivning

peripheral neuropathy

Datatyp

boolean

Alias
UMLS CUI [1]
C0031117

Similar models

Eligibility Stage IA Non-Small Cell Lung Carcinoma NCT02154399

Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
C1512693 (UMLS CUI)
non-small cell lung cancer
Item
known or suspected non-small cell lung cancer; patients without histologically or cytologically documented non-small cell lung cancer (nsclc) must be estimated by their physician to have at least 75% probability of having nsclc; the probability of malignancy will be predicted on the basis of known probabilities of individual clinical characteristics using a bayesian model
boolean
C0007131 (UMLS CUI [1])
clinical or pathologic stage i to iii
Item
clinical or pathologic stage i to iii; patients in whom pre-surgical staging has not definitively establish stage iv disease are eligible
boolean
C0027646 (UMLS CUI [1])
tumor mass size
Item
tumor mass at least 1.5 cm in maximum diameter must be present on computed tomography (ct) scan and must be included in the planned surgical biopsy or resection
boolean
C3273930 (UMLS CUI [1,1])
C0205099 (UMLS CUI [1,2])
surgical staging
Item
patient must be planning to undergo a surgical staging or treatment procedure (including mediastinoscopy, wedge resection, lobectomy, or pneumonectomy) and have the clinical and physiological status appropriate for this procedure
boolean
C0543467 (UMLS CUI [1])
performance status
Item
performance status 0-2
boolean
C1520224 (UMLS CUI [1])
bilirubin
Item
bilirubin within normal limits
boolean
C0005437 (UMLS CUI [1])
creatinine
Item
creatinine within normal limits or, if elevated, a creatinine clearance of at least 60 ml/min/m^2 (ef5 is primarily excreted via the kidney)
boolean
C0010294 (UMLS CUI [1])
C0373595 (UMLS CUI [2])
WBC
Item
white blood cell (wbc) > 2000/mm^3
boolean
C0023508 (UMLS CUI [1])
platelets
Item
platelets > 100,000/mm^3
boolean
C0005821 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
pregnancy or breast feeding
Item
pregnancy or breast feeding; a negative serum pregnancy test is required of any woman of childbearing potential prior to enrollment; pregnant women are excluded from this study; breastfeeding should be discontinued if the mother is treated with ef5
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
allergy to iv contrast dye
Item
allergy to iv contrast dye
boolean
C0020517 (UMLS CUI [1,1])
C0742795 (UMLS CUI [1,2])
peripheral neuropathy
Item
history of grade iii or iv peripheral neuropathy as defined by the national cancer institute (nci) common terminology criteria (ctc)
boolean
C0031117 (UMLS CUI [1])

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