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

Lien

https://clinicaltrials.gov/show/NCT00880386

Mots-clés

Versions (1)
  1. 15/03/2018 15/03/2018 -
Détendeur de droits

See clinicaltrials.gov

Téléchargé le

15 mars 2018

DOI

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Licence

Creative Commons BY 4.0
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Eligibility Dyspnea NCT00880386

Anglais

Eligibility Dyspnea NCT00880386

1 Formulaires  
  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

Type de données

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

Type de données

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

Type de données

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

Type de données

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

Type de données

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

Type de données

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

Type de données

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

Type de données

boolean

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

Tobacco use

Type de données

boolean

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

Pregnancy | Pregnancy, Planned | Breast Feeding

Type de données

boolean

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

Systolic Pressure

Type de données

boolean

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

Lung Transplantation

Type de données

boolean

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

Kidney Failure | Liver disease

Type de données

boolean

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

Clinic Visits Unable

Type de données

boolean

Alias
UMLS CUI [1,1]
C0008952
UMLS CUI [1,2]
C1299582
Retour au début de la page

Similar models

Eligibility Dyspnea NCT00880386

1 Formulaires
  1. StudyEvent: Eligibility
    1. Eligibility Dyspnea NCT00880386
Name
Type
Description | Question | Decode (Coded Value)
Type de données
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])
Retour au début de la page 

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