Information:
Error:
ID
39048
Description
Prevalence of Hyperventilation Syndrome in Difficult Asthma; ODM derived from: https://clinicaltrials.gov/show/NCT01862289
Link
https://clinicaltrials.gov/show/NCT01862289
Keywords
Versions (1)
- 11/23/19 11/23/19 -
Copyright Holder
See clinicaltrials.gov
Uploaded on
November 23, 2019
DOI
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License
Creative Commons BY 4.0
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Eligibility Difficult Asthma NCT01862289
Eligibility Difficult Asthma NCT01862289
- StudyEvent: Eligibility
Similar models
Eligibility Difficult Asthma NCT01862289
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Gender
Item
men and women,
boolean
C0079399 (UMLS CUI [1])
Age
Item
aged more than 18,
boolean
C0001779 (UMLS CUI [1])
Non-smoker | Former smoker Smoking cigarettes: ____ pack-years history
Item
non smokers for two years or longer, less than 10 pack/years smoking history,
boolean
C0337672 (UMLS CUI [1])
C0337671 (UMLS CUI [2,1])
C2230126 (UMLS CUI [2,2])
C0337671 (UMLS CUI [2,1])
C2230126 (UMLS CUI [2,2])
Asthma
Item
physician-diagnosed asthma,
boolean
C0004096 (UMLS CUI [1])
Asthma Uncontrolled Asthma control test score
Item
uncontrolled asthma with asthma control test (act) < 18,
boolean
C0004096 (UMLS CUI [1,1])
C0205318 (UMLS CUI [1,2])
C2733224 (UMLS CUI [1,3])
C0205318 (UMLS CUI [1,2])
C2733224 (UMLS CUI [1,3])
FEV1 Reversibility
Item
historical of fev1 reversibility,
boolean
C3830088 (UMLS CUI [1])
Inhaled steroid therapy | Beclomethasone U/day
Item
daily inhaled steroids treatment by at least 2000microg eq beclomethasone,
boolean
C4039912 (UMLS CUI [1])
C0004905 (UMLS CUI [2,1])
C0456683 (UMLS CUI [2,2])
C0004905 (UMLS CUI [2,1])
C0456683 (UMLS CUI [2,2])
Percent predicted FEV1
Item
forced expiratory volume in 1 second (fev1) > 50% predicted value
boolean
C0730561 (UMLS CUI [1])
Other chronic pulmonary disease
Item
other chronic pulmonary disease,
boolean
C0810290 (UMLS CUI [1])
Vocal Cord Dysfunction
Item
vocal cord dysfunction,
boolean
C0859897 (UMLS CUI [1])
Pregnancy
Item
pregnancy,
boolean
C0032961 (UMLS CUI [1])
Study Subject Participation Status | Interventional Study
Item
participation in another interventional research trial,
boolean
C2348568 (UMLS CUI [1])
C3274035 (UMLS CUI [2])
C3274035 (UMLS CUI [2])
infoInformed Consent Unable
Item
unable to provide consent,
boolean
C0021430 (UMLS CUI [1,1])
C1299582 (UMLS CUI [1,2])
C1299582 (UMLS CUI [1,2])
Exacerbation of asthma
Item
asthma exacerbation within the last 4 weeks
boolean
C0349790 (UMLS CUI [1])