ID

29287

Description

Losartan in Treating Pulmonary Fibrosis in Patients With Stage I, II, or III Non-Small Cell Lung Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT00880386

Link

https://clinicaltrials.gov/show/NCT00880386

Keywords

Versions (1)
  1. 3/15/18 3/15/18 -
Copyright Holder

See clinicaltrials.gov

Uploaded on

March 15, 2018

DOI

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License

Creative Commons BY 4.0
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Eligibility Dyspnea NCT00880386

English

Eligibility Dyspnea NCT00880386

1 forms  
  1. StudyEvent: Eligibility
    1. Eligibility Dyspnea NCT00880386
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
at least 18 years of age or older
Description

Age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
diagnosed with non-small cell lung cancer stage i, ii, iiia, or iiib
Description

Non-Small Cell Lung Carcinoma TNM clinical staging

Data type

boolean

Alias
UMLS CUI [1,1]
C0007131
UMLS CUI [1,2]
C3258246
diagnosis of radiation-induced pulmonary fibrosis (as defined by national cancer institute's common terminology criteria for adverse events [ctcae] v3.0 grade i to grade iii) and within 2 years of the last radiation therapy treatment
Description

Fibrosis of lung following radiation CTCAE Grades

Data type

boolean

Alias
UMLS CUI [1,1]
C0340126
UMLS CUI [1,2]
C1516728
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients with a pneumonectomy
Description

Pneumonectomy

Data type

boolean

Alias
UMLS CUI [1]
C0032284
allergy or allergic reaction to losartan or any other angiotensin ii receptor blocker
Description

Losartan allergy | Allergic Reaction Losartan | Allergy to angiotensin II receptor antagonist | Allergic Reaction Angiotensin II receptor antagonist

Data type

boolean

Alias
UMLS CUI [1]
C0571952
UMLS CUI [2,1]
C1527304
UMLS CUI [2,2]
C0126174
UMLS CUI [3]
C2585204
UMLS CUI [4,1]
C1527304
UMLS CUI [4,2]
C0521942
use of an angiotensin ii receptor blocker currently or within 6 months of study entry which include: losartan, valsartan, irbesartan, candesartan, cilexetil, eprosartan mesylate, and telmisartan
Description

Angiotensin II receptor antagonist | Losartan | valsartan | irbesartan | candesartan | candesartan cilexetil | Eprosartan mesylate | telmisartan

Data type

boolean

Alias
UMLS CUI [1]
C0521942
UMLS CUI [2]
C0126174
UMLS CUI [3]
C0216784
UMLS CUI [4]
C0288171
UMLS CUI [5]
C0717550
UMLS CUI [6]
C0527379
UMLS CUI [7]
C0772203
UMLS CUI [8]
C0248719
bilateral renal artery stenosis, hereditary or idiopathic angioedema, or uncontrolled hypotension
Description

Bilateral renal artery stenosis | Angioedemas, Hereditary | Idiopathic angioedema | Hypotension Uncontrolled

Data type

boolean

Alias
UMLS CUI [1]
C0856760
UMLS CUI [2]
C0019243
UMLS CUI [3]
C1304177
UMLS CUI [4,1]
C0020649
UMLS CUI [4,2]
C0205318
patients taking lithium
Description

Lithium

Data type

boolean

Alias
UMLS CUI [1]
C0023870
currently smoking or smoked within 6 months of study entry
Description

Tobacco use

Data type

boolean

Alias
UMLS CUI [1]
C0543414
pregnant, intending to become pregnant or breastfeeding
Description

Pregnancy | Pregnancy, Planned | Breast Feeding

Data type

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0032992
UMLS CUI [3]
C0006147
baseline systolic blood pressure < 100 mmhg
Description

Systolic Pressure

Data type

boolean

Alias
UMLS CUI [1]
C0871470
history of lung transplant
Description

Lung Transplantation

Data type

boolean

Alias
UMLS CUI [1]
C0024128
history of kidney failure or liver disease
Description

Kidney Failure | Liver disease

Data type

boolean

Alias
UMLS CUI [1]
C0035078
UMLS CUI [2]
C0023895
inability to attend clinic visits
Description

Clinic Visits Unable

Data type

boolean

Alias
UMLS CUI [1,1]
C0008952
UMLS CUI [1,2]
C1299582
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Similar models

Eligibility Dyspnea NCT00880386

1 forms
  1. StudyEvent: Eligibility
    1. Eligibility Dyspnea NCT00880386
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Age
Item
at least 18 years of age or older
boolean
C0001779 (UMLS CUI [1])
Non-Small Cell Lung Carcinoma TNM clinical staging
Item
diagnosed with non-small cell lung cancer stage i, ii, iiia, or iiib
boolean
C0007131 (UMLS CUI [1,1])
C3258246 (UMLS CUI [1,2])
Fibrosis of lung following radiation CTCAE Grades
Item
diagnosis of radiation-induced pulmonary fibrosis (as defined by national cancer institute's common terminology criteria for adverse events [ctcae] v3.0 grade i to grade iii) and within 2 years of the last radiation therapy treatment
boolean
C0340126 (UMLS CUI [1,1])
C1516728 (UMLS CUI [1,2])
Item Group
C0680251 (UMLS CUI)
Pneumonectomy
Item
patients with a pneumonectomy
boolean
C0032284 (UMLS CUI [1])
Losartan allergy | Allergic Reaction Losartan | Allergy to angiotensin II receptor antagonist | Allergic Reaction Angiotensin II receptor antagonist
Item
allergy or allergic reaction to losartan or any other angiotensin ii receptor blocker
boolean
C0571952 (UMLS CUI [1])
C1527304 (UMLS CUI [2,1])
C0126174 (UMLS CUI [2,2])
C2585204 (UMLS CUI [3])
C1527304 (UMLS CUI [4,1])
C0521942 (UMLS CUI [4,2])
Angiotensin II receptor antagonist | Losartan | valsartan | irbesartan | candesartan | candesartan cilexetil | Eprosartan mesylate | telmisartan
Item
use of an angiotensin ii receptor blocker currently or within 6 months of study entry which include: losartan, valsartan, irbesartan, candesartan, cilexetil, eprosartan mesylate, and telmisartan
boolean
C0521942 (UMLS CUI [1])
C0126174 (UMLS CUI [2])
C0216784 (UMLS CUI [3])
C0288171 (UMLS CUI [4])
C0717550 (UMLS CUI [5])
C0527379 (UMLS CUI [6])
C0772203 (UMLS CUI [7])
C0248719 (UMLS CUI [8])
Bilateral renal artery stenosis | Angioedemas, Hereditary | Idiopathic angioedema | Hypotension Uncontrolled
Item
bilateral renal artery stenosis, hereditary or idiopathic angioedema, or uncontrolled hypotension
boolean
C0856760 (UMLS CUI [1])
C0019243 (UMLS CUI [2])
C1304177 (UMLS CUI [3])
C0020649 (UMLS CUI [4,1])
C0205318 (UMLS CUI [4,2])
Lithium
Item
patients taking lithium
boolean
C0023870 (UMLS CUI [1])
Tobacco use
Item
currently smoking or smoked within 6 months of study entry
boolean
C0543414 (UMLS CUI [1])
Pregnancy | Pregnancy, Planned | Breast Feeding
Item
pregnant, intending to become pregnant or breastfeeding
boolean
C0032961 (UMLS CUI [1])
C0032992 (UMLS CUI [2])
C0006147 (UMLS CUI [3])
Systolic Pressure
Item
baseline systolic blood pressure < 100 mmhg
boolean
C0871470 (UMLS CUI [1])
Lung Transplantation
Item
history of lung transplant
boolean
C0024128 (UMLS CUI [1])
Kidney Failure | Liver disease
Item
history of kidney failure or liver disease
boolean
C0035078 (UMLS CUI [1])
C0023895 (UMLS CUI [2])
Clinic Visits Unable
Item
inability to attend clinic visits
boolean
C0008952 (UMLS CUI [1,1])
C1299582 (UMLS CUI [1,2])
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