ID

14562

Descripción

Genetics of Asthma - Bronchoscopy Studies; ODM derived from: https://clinicaltrials.gov/show/NCT00644514

Link

https://clinicaltrials.gov/show/NCT00644514

Palabras clave

Versiones (1)
  1. 21/4/16 21/4/16 -
Subido en

21 de abril de 2016

DOI

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Licencia

Creative Commons BY 4.0
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Eligibility Atopic Asthma NCT00644514

Inglés

Eligibility Atopic Asthma NCT00644514

1 formularios  
Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
allergic asthmatic, allergic non-asthmatic, or nonallergic nonasthmatic
Descripción

Allergic asthma | Allergic not Asthma | Not allergic Not Asthma

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0155877
UMLS CUI [2,1]
C0700624
UMLS CUI [2,2]
C1518422
UMLS CUI [2,3]
C0004096
UMLS CUI [3,1]
C1518422
UMLS CUI [3,2]
C0700624
UMLS CUI [3,3]
C1518422
UMLS CUI [3,4]
C0004096
willing/able to give informed consent & adhere to visit/protocol schedules.
Descripción

Informed Consent | Compliance behavior

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0021430
UMLS CUI [2]
C1321605
screening visit laboratory, c-xray, ekg, results within normal limits
Descripción

Laboratory results normal | Standard chest X-ray normal | ECG normal

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C1254595
UMLS CUI [1,2]
C0205307
UMLS CUI [2]
C0239026
UMLS CUI [3]
C0522054
women of childbearing potential must have a negative serum pregnancy test
Descripción

Childbearing Potential | Serum pregnancy test negative

Tipo de datos

boolean

Alias
UMLS CUI [1]
C3831118
UMLS CUI [2]
C0430061
screening pulmonary function testing above study criteria parameters
Descripción

Pulmonary function tests | Clinical Trial Eligibility Criteria

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0024119
UMLS CUI [2]
C1516637
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
systemic corticosteroid administration for asthma within the previous 90days
Descripción

systemic steroids | Asthma

Tipo de datos

boolean

Alias
UMLS CUI [1]
C2825233
UMLS CUI [2]
C0004096
antibiotic administration within the previous 30 days.
Descripción

Antibiotics

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0003232
viral respiratory infection within the previous 14 days.
Descripción

Viral respiratory infection

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0729531
history of severe asthma requiring intubation.
Descripción

Severe asthma | Intubation

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0581126
UMLS CUI [2]
C0021925
occupational exposure to hay or grain dust.
Descripción

Occupational Exposure Hay dust | Occupational Exposure Grain dust

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0028798
UMLS CUI [1,2]
C0450019
UMLS CUI [2,1]
C0028798
UMLS CUI [2,2]
C0304065
significant exposure history to cigarette smoke
Descripción

exposure to cigarette/cigar smoke

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1948106
past or present history of allergen immunotherapy to within the last 10 yrs
Descripción

Allergen Immunotherapy

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0162352
underlying illnesses that may result in altered lung function
Descripción

Illness Affecting Lung function

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0221423
UMLS CUI [1,2]
C0392760
UMLS CUI [1,3]
C0024119
students or employees under direct supervision by protocol investigators are ineligible
Descripción

student control clinical research investigator | Employee control clinical research investigator

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0038492
UMLS CUI [1,2]
C0243148
UMLS CUI [1,3]
C1552025
UMLS CUI [2,1]
C0599987
UMLS CUI [2,2]
C0243148
UMLS CUI [2,3]
C1552025
subjects allergic to medications used (or potentially used) in the study will be excluded.
Descripción

Hypersensitivity Pharmaceutical Preparations Clinical Research

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C0013227
UMLS CUI [1,3]
C0008972
subjects using aspirin will be excluded
Descripción

use; aspirin

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1388856
subjects who abuse alcohol or illicit substances will be excluded
Descripción

Substance Use Disorders

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0038586
medication use other than for asthma, allergies or contraception
Descripción

Pharmaceutical Preparations | Asthma | Hypersensitivity | Contraceptive methods

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0013227
UMLS CUI [2]
C0004096
UMLS CUI [3]
C0020517
UMLS CUI [4]
C0700589
other medical or psychological conditions which, in the opinion of the investigator, might create undue risk to the subject or interfere with the subject's ability to comply with the protocol requirements
Descripción

Disease Study Subject Participation Status Limited

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0012634
UMLS CUI [1,2]
C2348568
UMLS CUI [1,3]
C0439801
nursing mothers
Descripción

Breast Feeding Mother

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0006147
UMLS CUI [1,2]
C0026591
other investigational medication within the last 30 days
Descripción

Other Investigational New Drugs

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0205394
UMLS CUI [1,2]
C0013230
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Similar models

Eligibility Atopic Asthma NCT00644514

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
Allergic asthma | Allergic not Asthma | Not allergic Not Asthma
Item
allergic asthmatic, allergic non-asthmatic, or nonallergic nonasthmatic
boolean
C0155877 (UMLS CUI [1])
C0700624 (UMLS CUI [2,1])
C1518422 (UMLS CUI [2,2])
C0004096 (UMLS CUI [2,3])
C1518422 (UMLS CUI [3,1])
C0700624 (UMLS CUI [3,2])
C1518422 (UMLS CUI [3,3])
C0004096 (UMLS CUI [3,4])
Informed Consent | Compliance behavior
Item
willing/able to give informed consent & adhere to visit/protocol schedules.
boolean
C0021430 (UMLS CUI [1])
C1321605 (UMLS CUI [2])
Laboratory results normal | Standard chest X-ray normal | ECG normal
Item
screening visit laboratory, c-xray, ekg, results within normal limits
boolean
C1254595 (UMLS CUI [1,1])
C0205307 (UMLS CUI [1,2])
C0239026 (UMLS CUI [2])
C0522054 (UMLS CUI [3])
Childbearing Potential | Serum pregnancy test negative
Item
women of childbearing potential must have a negative serum pregnancy test
boolean
C3831118 (UMLS CUI [1])
C0430061 (UMLS CUI [2])
Pulmonary function tests | Clinical Trial Eligibility Criteria
Item
screening pulmonary function testing above study criteria parameters
boolean
C0024119 (UMLS CUI [1])
C1516637 (UMLS CUI [2])
Item Group
C0680251 (UMLS CUI)
systemic steroids | Asthma
Item
systemic corticosteroid administration for asthma within the previous 90days
boolean
C2825233 (UMLS CUI [1])
C0004096 (UMLS CUI [2])
Antibiotics
Item
antibiotic administration within the previous 30 days.
boolean
C0003232 (UMLS CUI [1])
Viral respiratory infection
Item
viral respiratory infection within the previous 14 days.
boolean
C0729531 (UMLS CUI [1])
Severe asthma | Intubation
Item
history of severe asthma requiring intubation.
boolean
C0581126 (UMLS CUI [1])
C0021925 (UMLS CUI [2])
Occupational Exposure Hay dust | Occupational Exposure Grain dust
Item
occupational exposure to hay or grain dust.
boolean
C0028798 (UMLS CUI [1,1])
C0450019 (UMLS CUI [1,2])
C0028798 (UMLS CUI [2,1])
C0304065 (UMLS CUI [2,2])
exposure to cigarette/cigar smoke
Item
significant exposure history to cigarette smoke
boolean
C1948106 (UMLS CUI [1])
Allergen Immunotherapy
Item
past or present history of allergen immunotherapy to within the last 10 yrs
boolean
C0162352 (UMLS CUI [1])
Illness Affecting Lung function
Item
underlying illnesses that may result in altered lung function
boolean
C0221423 (UMLS CUI [1,1])
C0392760 (UMLS CUI [1,2])
C0024119 (UMLS CUI [1,3])
student control clinical research investigator | Employee control clinical research investigator
Item
students or employees under direct supervision by protocol investigators are ineligible
boolean
C0038492 (UMLS CUI [1,1])
C0243148 (UMLS CUI [1,2])
C1552025 (UMLS CUI [1,3])
C0599987 (UMLS CUI [2,1])
C0243148 (UMLS CUI [2,2])
C1552025 (UMLS CUI [2,3])
Hypersensitivity Pharmaceutical Preparations Clinical Research
Item
subjects allergic to medications used (or potentially used) in the study will be excluded.
boolean
C0020517 (UMLS CUI [1,1])
C0013227 (UMLS CUI [1,2])
C0008972 (UMLS CUI [1,3])
use; aspirin
Item
subjects using aspirin will be excluded
boolean
C1388856 (UMLS CUI [1])
Substance Use Disorders
Item
subjects who abuse alcohol or illicit substances will be excluded
boolean
C0038586 (UMLS CUI [1])
Pharmaceutical Preparations | Asthma | Hypersensitivity | Contraceptive methods
Item
medication use other than for asthma, allergies or contraception
boolean
C0013227 (UMLS CUI [1])
C0004096 (UMLS CUI [2])
C0020517 (UMLS CUI [3])
C0700589 (UMLS CUI [4])
Disease Study Subject Participation Status Limited
Item
other medical or psychological conditions which, in the opinion of the investigator, might create undue risk to the subject or interfere with the subject's ability to comply with the protocol requirements
boolean
C0012634 (UMLS CUI [1,1])
C2348568 (UMLS CUI [1,2])
C0439801 (UMLS CUI [1,3])
Breast Feeding Mother
Item
nursing mothers
boolean
C0006147 (UMLS CUI [1,1])
C0026591 (UMLS CUI [1,2])
Other Investigational New Drugs
Item
other investigational medication within the last 30 days
boolean
C0205394 (UMLS CUI [1,1])
C0013230 (UMLS CUI [1,2])
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