Eligibility Asthma NCT00597064

  1. StudyEvent: Eligibility
    1. Eligibility Asthma NCT00597064
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
a documented clinical asthma history at least for a period of six months
Description

history of asthma

Data type

boolean

Alias
UMLS CUI [1,1]
C0262926
UMLS CUI [1,2]
C0004096
UMLS CUI [1,3]
C0040223
regular treatment (ic + laba) at least for a period of three months
Description

ics and laba

Data type

boolean

Alias
UMLS CUI [1]
C3248292
UMLS CUI [2]
C1373132
controlled symptoms score defined by gina 2002 criteria (daytime symptoms < 2 days a week and no night time symptoms in the last 15 days) or complete absence of chronic symptoms
Description

asthma symptom score

Data type

boolean

Alias
UMLS CUI [1]
C1273489
UMLS CUI [2]
C1276804
none or minimal exacerbations without emergency visits
Description

asthma exacerbation

Data type

boolean

Alias
UMLS CUI [1]
C0349790
UMLS CUI [2]
C0583237
absent or a minimal usage bronchodilator rescue, side effects of medication and limitation to exercises
Description

absent or a minimal usage bronchodilator rescue, side effects of medication and limitation to exercises

Data type

boolean

Alias
UMLS CUI [1]
C0578554
UMLS CUI [2]
C0392325
UMLS CUI [3,1]
C0015259
UMLS CUI [3,2]
C0439801
documented airway reversibility of 200 ml and 7% based on predicted values of vef1
Description

airway reversibility fev1

Data type

boolean

Alias
UMLS CUI [1,1]
C0748133
UMLS CUI [1,2]
C0449261
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
having a smoking history of 5 pack/years or more; having other known chronic pulmonary diseases; having side effect to oral corticosteroid
Description

smoking history chronic pulmonary diseases side effects to oral corticosteroid

Data type

boolean

Alias
UMLS CUI [1]
C1519384
UMLS CUI [2]
C1277691
UMLS CUI [3]
C0024115
UMLS CUI [4,1]
C0041755
UMLS CUI [4,2]
C0001617
having an upper or lower respiratory tract infection within 4 weeks of visit 0
Description

respiratory tract infection

Data type

boolean

Alias
UMLS CUI [1,1]
C0035243
UMLS CUI [1,2]
C0040223
unable to do the tests involved in the study.
Description

unable to do the tests involved in the study

Data type

boolean

Alias
UMLS CUI [1]
C1321605

Similar models

Eligibility Asthma NCT00597064

  1. StudyEvent: Eligibility
    1. Eligibility Asthma NCT00597064
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
history of asthma
Item
a documented clinical asthma history at least for a period of six months
boolean
C0262926 (UMLS CUI [1,1])
C0004096 (UMLS CUI [1,2])
C0040223 (UMLS CUI [1,3])
ics and laba
Item
regular treatment (ic + laba) at least for a period of three months
boolean
C3248292 (UMLS CUI [1])
C1373132 (UMLS CUI [2])
asthma symptom score
Item
controlled symptoms score defined by gina 2002 criteria (daytime symptoms < 2 days a week and no night time symptoms in the last 15 days) or complete absence of chronic symptoms
boolean
C1273489 (UMLS CUI [1])
C1276804 (UMLS CUI [2])
asthma exacerbation
Item
none or minimal exacerbations without emergency visits
boolean
C0349790 (UMLS CUI [1])
C0583237 (UMLS CUI [2])
absent or a minimal usage bronchodilator rescue, side effects of medication and limitation to exercises
Item
absent or a minimal usage bronchodilator rescue, side effects of medication and limitation to exercises
boolean
C0578554 (UMLS CUI [1])
C0392325 (UMLS CUI [2])
C0015259 (UMLS CUI [3,1])
C0439801 (UMLS CUI [3,2])
airway reversibility fev1
Item
documented airway reversibility of 200 ml and 7% based on predicted values of vef1
boolean
C0748133 (UMLS CUI [1,1])
C0449261 (UMLS CUI [1,2])
Item Group
C0680251 (UMLS CUI)
smoking history chronic pulmonary diseases side effects to oral corticosteroid
Item
having a smoking history of 5 pack/years or more; having other known chronic pulmonary diseases; having side effect to oral corticosteroid
boolean
C1519384 (UMLS CUI [1])
C1277691 (UMLS CUI [2])
C0024115 (UMLS CUI [3])
C0041755 (UMLS CUI [4,1])
C0001617 (UMLS CUI [4,2])
respiratory tract infection
Item
having an upper or lower respiratory tract infection within 4 weeks of visit 0
boolean
C0035243 (UMLS CUI [1,1])
C0040223 (UMLS CUI [1,2])
unable to do the tests involved in the study
Item
unable to do the tests involved in the study.
boolean
C1321605 (UMLS CUI [1])