Eligibility Asthma NCT00132834

  1. StudyEvent: Eligibility
    1. Eligibility Asthma NCT00132834
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI-1
C1512693
physician-diagnosed asthma
Description

asthma

Type de données

boolean

Alias
UMLS CUI [1]
C0004096
symptoms consistent with persistent asthma in the year prior to study entry
Description

persistent asthma

Type de données

boolean

Alias
UMLS CUI [1,1]
C3266628
UMLS CUI [1,2]
C0040223
able to speak and understand english
Description

english

Type de données

boolean

Alias
UMLS CUI [1]
C0376245
parent or guardian willing to provide informed consent
Description

informed consent

Type de données

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C0030551
Exclusion criteria
Description

Exclusion criteria

Alias
UMLS CUI-1
C0680251
diagnoses indicating other lung-related disorders (e.g., cystic fibrosis, bronchopulmonary dysplasia [bpd])
Description

lung disease

Type de données

boolean

Alias
UMLS CUI [1]
C0024115
allergy to latex
Description

allergy to latex

Type de données

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C0023115
smoker
Description

smoker

Type de données

boolean

Alias
UMLS CUI [1]
C0543414
albuterol use within 12 hours of study entry
Description

albuterol

Type de données

boolean

Alias
UMLS CUI [1,1]
C0001927
UMLS CUI [1,2]
C0040223
long-acting bronchodilator or leukotriene modifier use within 24 hours of study entry
Description

long-acting bronchodilator or leukotriene modifier

Type de données

boolean

Alias
UMLS CUI [1,1]
C2936789
UMLS CUI [1,2]
C0040223
unable to use the r-tube. more information on this criterion can be found in the dait icac-ebc protocol.
Description

r-tube

Type de données

boolean

exclusion criteria for part a participants: ics or oral corticosteroid use in the month prior to study entry
Description

ics or oral corticosteroid use

Type de données

boolean

Alias
UMLS CUI [1,1]
C3248292
UMLS CUI [1,2]
C0040223
UMLS CUI [2,1]
C3653473
UMLS CUI [2,2]
C0040223

Similar models

Eligibility Asthma NCT00132834

  1. StudyEvent: Eligibility
    1. Eligibility Asthma NCT00132834
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
Inclusion Criteria
C1512693 (UMLS CUI-1)
asthma
Item
physician-diagnosed asthma
boolean
C0004096 (UMLS CUI [1])
persistent asthma
Item
symptoms consistent with persistent asthma in the year prior to study entry
boolean
C3266628 (UMLS CUI [1,1])
C0040223 (UMLS CUI [1,2])
english
Item
able to speak and understand english
boolean
C0376245 (UMLS CUI [1])
informed consent
Item
parent or guardian willing to provide informed consent
boolean
C0021430 (UMLS CUI [1,1])
C0030551 (UMLS CUI [1,2])
Item Group
Exclusion criteria
C0680251 (UMLS CUI-1)
lung disease
Item
diagnoses indicating other lung-related disorders (e.g., cystic fibrosis, bronchopulmonary dysplasia [bpd])
boolean
C0024115 (UMLS CUI [1])
allergy to latex
Item
allergy to latex
boolean
C0020517 (UMLS CUI [1,1])
C0023115 (UMLS CUI [1,2])
smoker
Item
smoker
boolean
C0543414 (UMLS CUI [1])
albuterol
Item
albuterol use within 12 hours of study entry
boolean
C0001927 (UMLS CUI [1,1])
C0040223 (UMLS CUI [1,2])
long-acting bronchodilator or leukotriene modifier
Item
long-acting bronchodilator or leukotriene modifier use within 24 hours of study entry
boolean
C2936789 (UMLS CUI [1,1])
C0040223 (UMLS CUI [1,2])
r-tube
Item
unable to use the r-tube. more information on this criterion can be found in the dait icac-ebc protocol.
boolean
ics or oral corticosteroid use
Item
exclusion criteria for part a participants: ics or oral corticosteroid use in the month prior to study entry
boolean
C3248292 (UMLS CUI [1,1])
C0040223 (UMLS CUI [1,2])
C3653473 (UMLS CUI [2,1])
C0040223 (UMLS CUI [2,2])