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ID
14278
Beschrijving
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
Trefwoorden
Versies (1)
- 07-04-16 07-04-16 -
Houder van rechten
CC BY-NC 3.0
Geüploaded op
7 april 2016
DOI
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Licentie
Creative Commons BY-NC 3.0
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Eligibility Asthma NCT00291382
Eligibility Asthma NCT00291382
- StudyEvent: Eligibility
Similar models
Eligibility Asthma NCT00291382
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
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])
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])
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])
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])
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])
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])
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])
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])