ID

17931

Description

Iressa in Poor Performance Status Patients With Previously Untreated Advanced Non-Small Cell Lung Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT00193336

Link

https://clinicaltrials.gov/show/NCT00193336

Keywords

Versions (1)
  1. 10/10/16 10/10/16 -
Uploaded on

October 10, 2016

DOI

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License

Creative Commons BY 4.0
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Eligibility Lung Cancer NCT00193336

English

Eligibility Lung Cancer NCT00193336

1 forms  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
to be included in this study, you must meet the following criteria:
Description

criteria Fulfill

Data type

boolean

Alias
UMLS CUI [1,1]
C0243161
UMLS CUI [1,2]
C1550543
biopsy proven non-small cell lung cancer
Description

Non-Small Cell Lung Carcinoma | Biopsy

Data type

boolean

Alias
UMLS CUI [1]
C0007131
UMLS CUI [2]
C0005558
recurrent non-small cell lung cancer after previous surgery or radiation
Description

Non-small cell lung cancer recurrent | Operative Surgical Procedures | Therapeutic radiology procedure

Data type

boolean

Alias
UMLS CUI [1]
C0278517
UMLS CUI [2]
C0543467
UMLS CUI [3]
C1522449
advanced disease (stage iiib or iv)
Description

advanced disease | TNM clinical staging

Data type

boolean

Alias
UMLS CUI [1]
C0679246
UMLS CUI [2]
C3258246
no previous chemotherapy or biological therapy
Description

Prior Chemotherapy | Biological treatment

Data type

boolean

Alias
UMLS CUI [1]
C1514457
UMLS CUI [2]
C1531518
require significant assistance with activities of daily living
Description

Assisting with activity of daily living Significant Patient need for

Data type

boolean

Alias
UMLS CUI [1,1]
C0509063
UMLS CUI [1,2]
C0750502
UMLS CUI [1,3]
C0686904
measurable disease
Description

Measurable Disease

Data type

boolean

Alias
UMLS CUI [1]
C1513041
adequate bone marrow, liver and kidney function
Description

Bone Marrow function | Liver function | Normal renal function

Data type

boolean

Alias
UMLS CUI [1,1]
C0005953
UMLS CUI [1,2]
C0031843
UMLS CUI [2]
C0232741
UMLS CUI [3]
C0232805
give written informed consent
Description

Informed Consent

Data type

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
you cannot participate in this study if any of the following apply to you:
Description

Study Subject Participation Status

Data type

boolean

Alias
UMLS CUI [1]
C2348568
brain metastasis
Description

Metastatic malignant neoplasm to brain

Data type

boolean

Alias
UMLS CUI [1]
C0220650
meningeal metastasis
Description

Metastatic Malignant Neoplasm to the Leptomeninges

Data type

boolean

Alias
UMLS CUI [1]
C1704231
other uncontrolled malignancies
Description

Malignant Neoplasms Uncontrolled

Data type

boolean

Alias
UMLS CUI [1,1]
C0006826
UMLS CUI [1,2]
C0205318
women pregnant or lactating
Description

Pregnancy | Breast Feeding

Data type

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
no measurable disease outside previous radiation therapy field
Description

Involved-Field Radiation Therapy | Measurable Disease Extra-location

Data type

boolean

Alias
UMLS CUI [1]
C3826993
UMLS CUI [2,1]
C1513041
UMLS CUI [2,2]
C0442083
please note: there are additional inclusion/exclusion criteria. the study center will determine if you meet all of the criteria. if you do not qualify for the trial, study personnel will explain the reasons. if you do qualify, study personnel will explain the trial in detail and answer any questions you may have.
Description

criteria Study Protocol | Study Subject Participation Status

Data type

boolean

Alias
UMLS CUI [1,1]
C0243161
UMLS CUI [1,2]
C2348563
UMLS CUI [2]
C2348568
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Similar models

Eligibility Lung Cancer NCT00193336

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
criteria Fulfill
Item
to be included in this study, you must meet the following criteria:
boolean
C0243161 (UMLS CUI [1,1])
C1550543 (UMLS CUI [1,2])
Non-Small Cell Lung Carcinoma | Biopsy
Item
biopsy proven non-small cell lung cancer
boolean
C0007131 (UMLS CUI [1])
C0005558 (UMLS CUI [2])
Non-small cell lung cancer recurrent | Operative Surgical Procedures | Therapeutic radiology procedure
Item
recurrent non-small cell lung cancer after previous surgery or radiation
boolean
C0278517 (UMLS CUI [1])
C0543467 (UMLS CUI [2])
C1522449 (UMLS CUI [3])
advanced disease | TNM clinical staging
Item
advanced disease (stage iiib or iv)
boolean
C0679246 (UMLS CUI [1])
C3258246 (UMLS CUI [2])
Prior Chemotherapy | Biological treatment
Item
no previous chemotherapy or biological therapy
boolean
C1514457 (UMLS CUI [1])
C1531518 (UMLS CUI [2])
Assisting with activity of daily living Significant Patient need for
Item
require significant assistance with activities of daily living
boolean
C0509063 (UMLS CUI [1,1])
C0750502 (UMLS CUI [1,2])
C0686904 (UMLS CUI [1,3])
Measurable Disease
Item
measurable disease
boolean
C1513041 (UMLS CUI [1])
Bone Marrow function | Liver function | Normal renal function
Item
adequate bone marrow, liver and kidney function
boolean
C0005953 (UMLS CUI [1,1])
C0031843 (UMLS CUI [1,2])
C0232741 (UMLS CUI [2])
C0232805 (UMLS CUI [3])
Informed Consent
Item
give written informed consent
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Study Subject Participation Status
Item
you cannot participate in this study if any of the following apply to you:
boolean
C2348568 (UMLS CUI [1])
Metastatic malignant neoplasm to brain
Item
brain metastasis
boolean
C0220650 (UMLS CUI [1])
Metastatic Malignant Neoplasm to the Leptomeninges
Item
meningeal metastasis
boolean
C1704231 (UMLS CUI [1])
Malignant Neoplasms Uncontrolled
Item
other uncontrolled malignancies
boolean
C0006826 (UMLS CUI [1,1])
C0205318 (UMLS CUI [1,2])
Pregnancy | Breast Feeding
Item
women pregnant or lactating
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Involved-Field Radiation Therapy | Measurable Disease Extra-location
Item
no measurable disease outside previous radiation therapy field
boolean
C3826993 (UMLS CUI [1])
C1513041 (UMLS CUI [2,1])
C0442083 (UMLS CUI [2,2])
criteria Study Protocol | Study Subject Participation Status
Item
please note: there are additional inclusion/exclusion criteria. the study center will determine if you meet all of the criteria. if you do not qualify for the trial, study personnel will explain the reasons. if you do qualify, study personnel will explain the trial in detail and answer any questions you may have.
boolean
C0243161 (UMLS CUI [1,1])
C2348563 (UMLS CUI [1,2])
C2348568 (UMLS CUI [2])
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