ID

15614

Descrição

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

Link

https://clinicaltrials.gov/show/NCT02154399

Palavras-chave

  1. 05/06/2016 05/06/2016 -
Transferido a

5 de junho de 2016

DOI

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Licença

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
Descrição

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
Descrição

non-small cell lung cancer

Tipo de dados

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
Descrição

clinical or pathologic stage i to iii

Tipo de dados

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
Descrição

tumor mass size

Tipo de dados

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
Descrição

surgical staging

Tipo de dados

boolean

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

performance status

Tipo de dados

boolean

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

bilirubin

Tipo de dados

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)
Descrição

creatinine

Tipo de dados

boolean

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

WBC

Tipo de dados

boolean

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

platelets

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0005821
Exclusion Criteria
Descrição

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
Descrição

pregnancy or breast feeding

Tipo de dados

boolean

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

allergy to iv contrast dye

Tipo de dados

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)
Descrição

peripheral neuropathy

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0031117

Similar models

Eligibility Stage IA Non-Small Cell Lung Carcinoma NCT02154399

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
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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