Eligibility Asthma NCT00543686

  1. StudyEvent: Eligibility
    1. Eligibility Asthma NCT00543686
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
male or female patients age 4 -6 years
Description

age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
diagnosis of mild intermittent bronchial asthma (step i-ii) in the past 6 - 12 months as stated by the investigator:
Description

mild intermittent asthma

Data type

boolean

Alias
UMLS CUI [1]
C1960045
use of inhaled beta-2-agonists < 1/week (max 3 puff /d)
Description

inhaled beta-2-agonists

Data type

boolean

Alias
UMLS CUI [1,1]
C1373132
UMLS CUI [1,2]
C0001559
exacerbation-free interval > 4 weeks prior to visit 1
Description

exacerbation-free interval

Data type

boolean

Alias
UMLS CUI [1,1]
C0349790
UMLS CUI [1,2]
C0040223
the written informed consent of parents after received written and oral information about the aim, purpose and risks of the study must be present
Description

written informed consent

Data type

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
asthma severity ≥ step 2
Description

asthma severity

Data type

boolean

Alias
UMLS CUI [1]
C0581122
severe concomitant diseases
Description

severe concomitant diseases

Data type

boolean

Alias
UMLS CUI [1]
C0009488
suspected non-compliance
Description

suspected non-compliance

Data type

boolean

Alias
UMLS CUI [1]
C1321605
age below 4 and age above 7 years
Description

age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
last study participation < 30 days
Description

last study participation

Data type

boolean

Alias
UMLS CUI [1,1]
C2348568
UMLS CUI [1,2]
C0040223

Similar models

Eligibility Asthma NCT00543686

  1. StudyEvent: Eligibility
    1. Eligibility Asthma NCT00543686
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
age
Item
male or female patients age 4 -6 years
boolean
C0001779 (UMLS CUI [1])
mild intermittent asthma
Item
diagnosis of mild intermittent bronchial asthma (step i-ii) in the past 6 - 12 months as stated by the investigator:
boolean
C1960045 (UMLS CUI [1])
inhaled beta-2-agonists
Item
use of inhaled beta-2-agonists < 1/week (max 3 puff /d)
boolean
C1373132 (UMLS CUI [1,1])
C0001559 (UMLS CUI [1,2])
exacerbation-free interval
Item
exacerbation-free interval > 4 weeks prior to visit 1
boolean
C0349790 (UMLS CUI [1,1])
C0040223 (UMLS CUI [1,2])
written informed consent
Item
the written informed consent of parents after received written and oral information about the aim, purpose and risks of the study must be present
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
asthma severity
Item
asthma severity ≥ step 2
boolean
C0581122 (UMLS CUI [1])
severe concomitant diseases
Item
severe concomitant diseases
boolean
C0009488 (UMLS CUI [1])
suspected non-compliance
Item
suspected non-compliance
boolean
C1321605 (UMLS CUI [1])
age
Item
age below 4 and age above 7 years
boolean
C0001779 (UMLS CUI [1])
last study participation
Item
last study participation < 30 days
boolean
C2348568 (UMLS CUI [1,1])
C0040223 (UMLS CUI [1,2])