ID

14278

Description

Airway Hyper-responsiveness Study In Asthma Using Salmeterol/Fluticasone Propionate Combination Product; ODM derived from: https://clinicaltrials.gov/show/NCT00291382

Link

https://clinicaltrials.gov/show/NCT00291382

Keywords

Versions (1)
  1. 4/7/16 4/7/16 -
Copyright Holder

CC BY-NC 3.0

Uploaded on

April 7, 2016

DOI

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License

Creative Commons BY-NC 3.0
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Eligibility Asthma NCT00291382

English

Eligibility Asthma NCT00291382

1 forms  
  1. StudyEvent: Eligibility
    1. Eligibility Asthma NCT00291382
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
history of asthma of at least 6 months.
Description

history of asthma

Data type

boolean

Alias
UMLS CUI [1,1]
C0262926
UMLS CUI [1,2]
C0004096
UMLS CUI [1,3]
C0040223
subjects who have received fluticasone propionate at a dose of 100 mcg bd to 250 mcg bd or equivalent with or without a long acting beta2-agonist for at least 4 weeks before the start of the run-in period, at a constant dose.
Description

fluticasone propionate

Data type

boolean

Alias
UMLS CUI [1]
C0117996
UMLS CUI [2]
C2936789
subjects who are able to understand and complete an electronic diary card.
Description

able to understand and complete an electronic diary card

Data type

boolean

Alias
UMLS CUI [1]
C1321605
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
subjects who have been hospitalized for their asthma within 4 weeks of study entry.
Description

hospitalization

Data type

boolean

Alias
UMLS CUI [1,1]
C0019993
UMLS CUI [1,2]
C0040223
subjects who had an acute upper respiratory tract infection within 4 weeks or a lower respiratory tract infection within 4 weeks prior to study entry.
Description

respiratory tract infection

Data type

boolean

Alias
UMLS CUI [1,1]
C0035243
UMLS CUI [1,2]
C0040223
subjects who received oral, parental or depot corticosteroids within 4 weeks prior to study entry.
Description

corticosteroids

Data type

boolean

Alias
UMLS CUI [1,1]
C0001617
UMLS CUI [1,2]
C0040223
subjects who have a known respiratory disorder other than asthma and/or systemic/thoracic abnormalities which influence normal lung function.
Description

respiratory disorders or other abnormalities influencing normal lung function

Data type

boolean

Alias
UMLS CUI [1]
C0035204
UMLS CUI [2,1]
C0024119
UMLS CUI [2,2]
C0439801
UMLS CUI [2,3]
C0009488
subjects who have more than 5 pack years.
Description

pack years

Data type

boolean

Alias
UMLS CUI [1]
C1277691
subjects who currently smoke.
Description

current smoker

Data type

boolean

Alias
UMLS CUI [1]
C3241966
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Similar models

Eligibility Asthma NCT00291382

1 forms
  1. StudyEvent: Eligibility
    1. Eligibility Asthma NCT00291382
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
history of asthma
Item
history of asthma of at least 6 months.
boolean
C0262926 (UMLS CUI [1,1])
C0004096 (UMLS CUI [1,2])
C0040223 (UMLS CUI [1,3])
fluticasone propionate
Item
subjects who have received fluticasone propionate at a dose of 100 mcg bd to 250 mcg bd or equivalent with or without a long acting beta2-agonist for at least 4 weeks before the start of the run-in period, at a constant dose.
boolean
C0117996 (UMLS CUI [1])
C2936789 (UMLS CUI [2])
able to understand and complete an electronic diary card
Item
subjects who are able to understand and complete an electronic diary card.
boolean
C1321605 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
hospitalization
Item
subjects who have been hospitalized for their asthma within 4 weeks of study entry.
boolean
C0019993 (UMLS CUI [1,1])
C0040223 (UMLS CUI [1,2])
respiratory tract infection
Item
subjects who had an acute upper respiratory tract infection within 4 weeks or a lower respiratory tract infection within 4 weeks prior to study entry.
boolean
C0035243 (UMLS CUI [1,1])
C0040223 (UMLS CUI [1,2])
corticosteroids
Item
subjects who received oral, parental or depot corticosteroids within 4 weeks prior to study entry.
boolean
C0001617 (UMLS CUI [1,1])
C0040223 (UMLS CUI [1,2])
respiratory disorders or other abnormalities influencing normal lung function
Item
subjects who have a known respiratory disorder other than asthma and/or systemic/thoracic abnormalities which influence normal lung function.
boolean
C0035204 (UMLS CUI [1])
C0024119 (UMLS CUI [2,1])
C0439801 (UMLS CUI [2,2])
C0009488 (UMLS CUI [2,3])
pack years
Item
subjects who have more than 5 pack years.
boolean
C1277691 (UMLS CUI [1])
current smoker
Item
subjects who currently smoke.
boolean
C3241966 (UMLS CUI [1])
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