ID

14419

Description

Study of the Mechanisms of Asthma; ODM derived from: https://clinicaltrials.gov/show/NCT00595153

Link

https://clinicaltrials.gov/show/NCT00595153

Keywords

Versions (1)
  1. 4/14/16 4/14/16 -
Copyright Holder

CC BY-NC 3.0

Uploaded on

April 14, 2016

DOI

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License

Creative Commons BY-NC 3.0
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Eligibility Asthma NCT00595153

English

Eligibility Asthma NCT00595153

1 forms  
  1. StudyEvent: Eligibility
    1. Eligibility Asthma NCT00595153
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
group c:
Description

group

Data type

boolean

Alias
UMLS CUI [1]
C1257890
male and female subjects between the ages of 18 and 70 years
Description

age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
history of asthma
Description

history of asthma

Data type

boolean

Alias
UMLS CUI [1,1]
C0262926
UMLS CUI [1,2]
C0004096
continuous treatment with inhaled corticosteroids for at least the 6-week
Description

inhaled corticosteroids

Data type

boolean

Alias
UMLS CUI [1,1]
C2065041
UMLS CUI [1,2]
C0040223
hyperreactivity to methacholine (provocative concentration of methacholine causing a 20% drop in forced expiratory volume in 1 second (pc20 fev1) methacholine ≤ 16.0 mg/ml).
Description

hyperreactivity to methacholine

Data type

boolean

Alias
UMLS CUI [1]
C1096470
UMLS CUI [2]
C0748133
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
history of asthma
Description

history of asthma

Data type

boolean

Alias
UMLS CUI [1,1]
C0262926
UMLS CUI [1,2]
C0004096
no use of oral or inhaled corticosteroids for the treatment of asthma in the past 6 weeks
Description

oral or inhaled corticosteroids

Data type

boolean

Alias
UMLS CUI [1]
C2065041
UMLS CUI [2,1]
C0001617
UMLS CUI [2,2]
C0442027
UMLS CUI [3]
C0040223
hyperreactivity to methacholine (pc20 fev1 methacholine ≤ 8.0 mg/ml).
Description

hyperreactivity to methacholine

Data type

boolean

Alias
UMLS CUI [1]
C1096470
UMLS CUI [2]
C0748133
at least one of the following symptoms, beta agonist use, or fev1 criteria:
Description

symptoms beta agonist use or fev1

Data type

boolean

Alias
UMLS CUI [1]
C1457887
UMLS CUI [2]
C0001644
UMLS CUI [3]
C0748133
asthma symptoms on at least two days per week; or
Description

asthma symptoms

Data type

boolean

Alias
UMLS CUI [1,1]
C0004096
UMLS CUI [1,2]
C1457887
beta agonist use on at least two days per week; or
Description

beta agonist use

Data type

boolean

Alias
UMLS CUI [1]
C0001644
forced expiratory volume in 1 second (fev1) < 85% predicted
Description

fev1

Data type

boolean

Alias
UMLS CUI [1]
C0748133
subjects must be non-smokers (patients who have never smoked or patients who have not smoked for 1 year and have a total pack-year smoking history < 15 packs).
Description

non-smokers smoking history

Data type

boolean

Alias
UMLS CUI [1]
C0337672
UMLS CUI [2]
C1519384
UMLS CUI [3]
C1277691
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Similar models

Eligibility Asthma NCT00595153

1 forms
  1. StudyEvent: Eligibility
    1. Eligibility Asthma NCT00595153
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
group
Item
group c:
boolean
C1257890 (UMLS CUI [1])
age
Item
male and female subjects between the ages of 18 and 70 years
boolean
C0001779 (UMLS CUI [1])
history of asthma
Item
history of asthma
boolean
C0262926 (UMLS CUI [1,1])
C0004096 (UMLS CUI [1,2])
inhaled corticosteroids
Item
continuous treatment with inhaled corticosteroids for at least the 6-week
boolean
C2065041 (UMLS CUI [1,1])
C0040223 (UMLS CUI [1,2])
hyperreactivity to methacholine
Item
hyperreactivity to methacholine (provocative concentration of methacholine causing a 20% drop in forced expiratory volume in 1 second (pc20 fev1) methacholine ≤ 16.0 mg/ml).
boolean
C1096470 (UMLS CUI [1])
C0748133 (UMLS CUI [2])
Item Group
C0680251 (UMLS CUI)
history of asthma
Item
history of asthma
boolean
C0262926 (UMLS CUI [1,1])
C0004096 (UMLS CUI [1,2])
oral or inhaled corticosteroids
Item
no use of oral or inhaled corticosteroids for the treatment of asthma in the past 6 weeks
boolean
C2065041 (UMLS CUI [1])
C0001617 (UMLS CUI [2,1])
C0442027 (UMLS CUI [2,2])
C0040223 (UMLS CUI [3])
hyperreactivity to methacholine
Item
hyperreactivity to methacholine (pc20 fev1 methacholine ≤ 8.0 mg/ml).
boolean
C1096470 (UMLS CUI [1])
C0748133 (UMLS CUI [2])
symptoms beta agonist use or fev1
Item
at least one of the following symptoms, beta agonist use, or fev1 criteria:
boolean
C1457887 (UMLS CUI [1])
C0001644 (UMLS CUI [2])
C0748133 (UMLS CUI [3])
asthma symptoms
Item
asthma symptoms on at least two days per week; or
boolean
C0004096 (UMLS CUI [1,1])
C1457887 (UMLS CUI [1,2])
beta agonist use
Item
beta agonist use on at least two days per week; or
boolean
C0001644 (UMLS CUI [1])
fev1
Item
forced expiratory volume in 1 second (fev1) < 85% predicted
boolean
C0748133 (UMLS CUI [1])
non-smokers smoking history
Item
subjects must be non-smokers (patients who have never smoked or patients who have not smoked for 1 year and have a total pack-year smoking history < 15 packs).
boolean
C0337672 (UMLS CUI [1])
C1519384 (UMLS CUI [2])
C1277691 (UMLS CUI [3])
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