ID

22191

Descripción

A Study of Avastin (Bevacizumab) in Patients With Non-Squamous Non-Small Cell Lung Cancer (NSCLC); ODM derived from: https://clinicaltrials.gov/show/NCT00806923

Link

https://clinicaltrials.gov/show/NCT00806923

Palabras clave

Versiones (1)
  1. 22/5/17 22/5/17 -
Subido en

22 de mayo de 2017

DOI

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Licencia

Creative Commons BY 4.0
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Eligibility Non-Squamous Non-Small Cell Lung Cancer NCT00806923

Inglés

Eligibility Non-Squamous Non-Small Cell Lung Cancer NCT00806923

1 formularios  
Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
adult patients, >=18 years of age;
Descripción

Adult | Age

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0001675
UMLS CUI [2]
C0001779
documented inoperable, locally advanced, metastatic or recurrent non-squamous nsclc;
Descripción

Nonsquamous nonsmall cell neoplasm of lung Inoperable | Nonsquamous nonsmall cell neoplasm of lung Advanced Local | Nonsquamous nonsmall cell neoplasm of lung metastatic | Nonsquamous nonsmall cell neoplasm of lung Recurrent

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C2585890
UMLS CUI [1,2]
C0205187
UMLS CUI [2,1]
C2585890
UMLS CUI [2,2]
C0205179
UMLS CUI [2,3]
C0205276
UMLS CUI [3,1]
C2585890
UMLS CUI [3,2]
C1522484
UMLS CUI [4,1]
C2585890
UMLS CUI [4,2]
C2945760
adequate liver and kidney function;
Descripción

Liver function | Renal function

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0232741
UMLS CUI [2]
C0232804
women of childbearing potential must have a negative serum pregnancy test within 7 days of starting study treatment.
Descripción

Childbearing Potential Serum pregnancy test negative

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C3831118
UMLS CUI [1,2]
C0430061
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
prior chemotherapy or treatment with another systemic cancer therapy;
Descripción

Chemotherapy | Cancer treatment Systemic

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0392920
UMLS CUI [2,1]
C0920425
UMLS CUI [2,2]
C0205373
surgery (including open biopsy), significant traumatic injury, or radiotherapy within the last 4 weeks prior to first dose of study treatment;
Descripción

Operative Surgical Procedures | Incisional biopsy | Traumatic injury | Therapeutic radiology procedure

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0543467
UMLS CUI [2]
C0184922
UMLS CUI [3]
C3263723
UMLS CUI [4]
C1522449
brain metastasis or spinal cord compression;
Descripción

Metastatic malignant neoplasm to brain | Compression of spinal cord

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0220650
UMLS CUI [2]
C0037926
fertile men, and women of childbearing potential, not using adequate contraception;
Descripción

Gender Fertility Contraceptive methods Lacking | Childbearing Potential Contraceptive methods Lacking

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0079399
UMLS CUI [1,2]
C0015895
UMLS CUI [1,3]
C0700589
UMLS CUI [1,4]
C0332268
UMLS CUI [2,1]
C3831118
UMLS CUI [2,2]
C0700589
UMLS CUI [2,3]
C0332268
treatment with any other investigational agent, or participation in another clinical trial, within 30 days prior to entering the study.
Descripción

Investigational New Drugs | Study Subject Participation Status

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0013230
UMLS CUI [2]
C2348568
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Similar models

Eligibility Non-Squamous Non-Small Cell Lung Cancer NCT00806923

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
Adult | Age
Item
adult patients, >=18 years of age;
boolean
C0001675 (UMLS CUI [1])
C0001779 (UMLS CUI [2])
Nonsquamous nonsmall cell neoplasm of lung Inoperable | Nonsquamous nonsmall cell neoplasm of lung Advanced Local | Nonsquamous nonsmall cell neoplasm of lung metastatic | Nonsquamous nonsmall cell neoplasm of lung Recurrent
Item
documented inoperable, locally advanced, metastatic or recurrent non-squamous nsclc;
boolean
C2585890 (UMLS CUI [1,1])
C0205187 (UMLS CUI [1,2])
C2585890 (UMLS CUI [2,1])
C0205179 (UMLS CUI [2,2])
C0205276 (UMLS CUI [2,3])
C2585890 (UMLS CUI [3,1])
C1522484 (UMLS CUI [3,2])
C2585890 (UMLS CUI [4,1])
C2945760 (UMLS CUI [4,2])
Liver function | Renal function
Item
adequate liver and kidney function;
boolean
C0232741 (UMLS CUI [1])
C0232804 (UMLS CUI [2])
Childbearing Potential Serum pregnancy test negative
Item
women of childbearing potential must have a negative serum pregnancy test within 7 days of starting study treatment.
boolean
C3831118 (UMLS CUI [1,1])
C0430061 (UMLS CUI [1,2])
Item Group
C0680251 (UMLS CUI)
Chemotherapy | Cancer treatment Systemic
Item
prior chemotherapy or treatment with another systemic cancer therapy;
boolean
C0392920 (UMLS CUI [1])
C0920425 (UMLS CUI [2,1])
C0205373 (UMLS CUI [2,2])
Operative Surgical Procedures | Incisional biopsy | Traumatic injury | Therapeutic radiology procedure
Item
surgery (including open biopsy), significant traumatic injury, or radiotherapy within the last 4 weeks prior to first dose of study treatment;
boolean
C0543467 (UMLS CUI [1])
C0184922 (UMLS CUI [2])
C3263723 (UMLS CUI [3])
C1522449 (UMLS CUI [4])
Metastatic malignant neoplasm to brain | Compression of spinal cord
Item
brain metastasis or spinal cord compression;
boolean
C0220650 (UMLS CUI [1])
C0037926 (UMLS CUI [2])
Gender Fertility Contraceptive methods Lacking | Childbearing Potential Contraceptive methods Lacking
Item
fertile men, and women of childbearing potential, not using adequate contraception;
boolean
C0079399 (UMLS CUI [1,1])
C0015895 (UMLS CUI [1,2])
C0700589 (UMLS CUI [1,3])
C0332268 (UMLS CUI [1,4])
C3831118 (UMLS CUI [2,1])
C0700589 (UMLS CUI [2,2])
C0332268 (UMLS CUI [2,3])
Investigational New Drugs | Study Subject Participation Status
Item
treatment with any other investigational agent, or participation in another clinical trial, within 30 days prior to entering the study.
boolean
C0013230 (UMLS CUI [1])
C2348568 (UMLS CUI [2])
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