ID

21533

Descripción

Bevacizumab and Carboplatin/Paclitaxel and Radiation in Non-Small Cell Lung Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT00578149

Link

https://clinicaltrials.gov/show/NCT00578149

Palabras clave

  1. 26/4/17 26/4/17 -
Subido en

26 de abril de 2017

DOI

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Licencia

Creative Commons BY 4.0

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Eligibility Non-Small Cell Lung Cancer NCT00578149

Eligibility Non-Small Cell Lung Cancer NCT00578149

Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
histologically confirmed non-small cell lung cancer (nsclc) that have been evaluated and determined not to be candidates for surgical resection as part of their definitive management of stage iii disease.
Descripción

Non-small cell lung cancer, operability, tumor stage

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0007131
UMLS CUI [2]
C0205188
UMLS CUI [3]
C1300072
age 18 years or older
Descripción

Age

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0001779
ecog performance status of 0-1
Descripción

ECOG Performance Status

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1520224
life expectancy of greater than six months
Descripción

Life Expectancy

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0023671
normal organ and marrow function
Descripción

Organ and bone marrow function

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0678852
UMLS CUI [2]
C0005953
women and men of child-bearing potential must agree to use adequate contraception
Descripción

Contraceptive methods

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0700589
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
prior chemotherapy or thoracic radiation therapy
Descripción

Prior Chemotherapy or Radiation

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0279134
UMLS CUI [2]
C1514457
squamous histology or any histology in close proximity to a major vessel
Descripción

Histological finding and tumor site

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0449575
UMLS CUI [2]
C0475445
active hemoptysis
Descripción

Hemoptysis

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0019079
history of hypercoagulability
Descripción

Hypercoagulability

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0398623
known distant metastatic disease
Descripción

Metastatic disease

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0027627
history of allergic reactions attributed to compounds with similar chemical or biological composition to bevacizumab, carboplatin, paclitaxel or other agents used in this study
Descripción

Hypersensitivity to bevacizumab, carboplatin, paclitaxel or other agents used in this study

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C0796392
UMLS CUI [2,1]
C0020517
UMLS CUI [2,2]
C0079083
UMLS CUI [3,1]
C0020517
UMLS CUI [3,2]
C0144576
UMLS CUI [4,1]
C0020517
UMLS CUI [4,2]
C0304229
patients with uncontrolled intercurrent illness
Descripción

Comorbidity

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0009488
pregnant women
Descripción

Pregnancy

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0032961
major surgical procedure, open biopsy, or significant traumatic injury with in 28 days prior to day 0
Descripción

Major surgical procedure, open biopsy, or significant traumatic injury

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0543467
UMLS CUI [2]
C0184922
UMLS CUI [3]
C3263723
minor surgical procedure within 7 days to day 0
Descripción

Minor surgical procedure

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0038904
hiv-positive patients receiving combination anti-retroviral therapy.
Descripción

HIV therapy

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0920551
non-skin cancer malignancy in the past 5 years.
Descripción

Prior malignancy

Tipo de datos

boolean

Alias
UMLS CUI [1]
C2735088

Similar models

Eligibility Non-Small Cell Lung Cancer NCT00578149

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
Non-small cell lung cancer, operability, tumor stage
Item
histologically confirmed non-small cell lung cancer (nsclc) that have been evaluated and determined not to be candidates for surgical resection as part of their definitive management of stage iii disease.
boolean
C0007131 (UMLS CUI [1])
C0205188 (UMLS CUI [2])
C1300072 (UMLS CUI [3])
Age
Item
age 18 years or older
boolean
C0001779 (UMLS CUI [1])
ECOG Performance Status
Item
ecog performance status of 0-1
boolean
C1520224 (UMLS CUI [1])
Life Expectancy
Item
life expectancy of greater than six months
boolean
C0023671 (UMLS CUI [1])
Organ and bone marrow function
Item
normal organ and marrow function
boolean
C0678852 (UMLS CUI [1])
C0005953 (UMLS CUI [2])
Contraceptive methods
Item
women and men of child-bearing potential must agree to use adequate contraception
boolean
C0700589 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Prior Chemotherapy or Radiation
Item
prior chemotherapy or thoracic radiation therapy
boolean
C0279134 (UMLS CUI [1])
C1514457 (UMLS CUI [2])
Histological finding and tumor site
Item
squamous histology or any histology in close proximity to a major vessel
boolean
C0449575 (UMLS CUI [1])
C0475445 (UMLS CUI [2])
Hemoptysis
Item
active hemoptysis
boolean
C0019079 (UMLS CUI [1])
Hypercoagulability
Item
history of hypercoagulability
boolean
C0398623 (UMLS CUI [1])
Metastatic disease
Item
known distant metastatic disease
boolean
C0027627 (UMLS CUI [1])
Hypersensitivity to bevacizumab, carboplatin, paclitaxel or other agents used in this study
Item
history of allergic reactions attributed to compounds with similar chemical or biological composition to bevacizumab, carboplatin, paclitaxel or other agents used in this study
boolean
C0020517 (UMLS CUI [1,1])
C0796392 (UMLS CUI [1,2])
C0020517 (UMLS CUI [2,1])
C0079083 (UMLS CUI [2,2])
C0020517 (UMLS CUI [3,1])
C0144576 (UMLS CUI [3,2])
C0020517 (UMLS CUI [4,1])
C0304229 (UMLS CUI [4,2])
Comorbidity
Item
patients with uncontrolled intercurrent illness
boolean
C0009488 (UMLS CUI [1])
Pregnancy
Item
pregnant women
boolean
C0032961 (UMLS CUI [1])
Major surgical procedure, open biopsy, or significant traumatic injury
Item
major surgical procedure, open biopsy, or significant traumatic injury with in 28 days prior to day 0
boolean
C0543467 (UMLS CUI [1])
C0184922 (UMLS CUI [2])
C3263723 (UMLS CUI [3])
Minor surgical procedure
Item
minor surgical procedure within 7 days to day 0
boolean
C0038904 (UMLS CUI [1])
HIV therapy
Item
hiv-positive patients receiving combination anti-retroviral therapy.
boolean
C0920551 (UMLS CUI [1])
Prior malignancy
Item
non-skin cancer malignancy in the past 5 years.
boolean
C2735088 (UMLS CUI [1])

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