ID

39048

Beschreibung

Prevalence of Hyperventilation Syndrome in Difficult Asthma; ODM derived from: https://clinicaltrials.gov/show/NCT01862289

Link

https://clinicaltrials.gov/show/NCT01862289

Stichworte

  1. 23.11.19 23.11.19 -
Rechteinhaber

See clinicaltrials.gov

Hochgeladen am

23. November 2019

DOI

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Lizenz

Creative Commons BY 4.0

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Eligibility Difficult Asthma NCT01862289

Eligibility Difficult Asthma NCT01862289

Inclusion Criteria
Beschreibung

Inclusion Criteria

Alias
UMLS CUI
C1512693
men and women,
Beschreibung

Gender

Datentyp

boolean

Alias
UMLS CUI [1]
C0079399
aged more than 18,
Beschreibung

Age

Datentyp

boolean

Alias
UMLS CUI [1]
C0001779
non smokers for two years or longer, less than 10 pack/years smoking history,
Beschreibung

Non-smoker | Former smoker Smoking cigarettes: ____ pack-years history

Datentyp

boolean

Alias
UMLS CUI [1]
C0337672
UMLS CUI [2,1]
C0337671
UMLS CUI [2,2]
C2230126
physician-diagnosed asthma,
Beschreibung

Asthma

Datentyp

boolean

Alias
UMLS CUI [1]
C0004096
uncontrolled asthma with asthma control test (act) < 18,
Beschreibung

Asthma Uncontrolled Asthma control test score

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0004096
UMLS CUI [1,2]
C0205318
UMLS CUI [1,3]
C2733224
historical of fev1 reversibility,
Beschreibung

FEV1 Reversibility

Datentyp

boolean

Alias
UMLS CUI [1]
C3830088
daily inhaled steroids treatment by at least 2000microg eq beclomethasone,
Beschreibung

Inhaled steroid therapy | Beclomethasone U/day

Datentyp

boolean

Alias
UMLS CUI [1]
C4039912
UMLS CUI [2,1]
C0004905
UMLS CUI [2,2]
C0456683
forced expiratory volume in 1 second (fev1) > 50% predicted value
Beschreibung

Percent predicted FEV1

Datentyp

boolean

Alias
UMLS CUI [1]
C0730561
Exclusion Criteria
Beschreibung

Exclusion Criteria

Alias
UMLS CUI
C0680251
other chronic pulmonary disease,
Beschreibung

Other chronic pulmonary disease

Datentyp

boolean

Alias
UMLS CUI [1]
C0810290
vocal cord dysfunction,
Beschreibung

Vocal Cord Dysfunction

Datentyp

boolean

Alias
UMLS CUI [1]
C0859897
pregnancy,
Beschreibung

Pregnancy

Datentyp

boolean

Alias
UMLS CUI [1]
C0032961
participation in another interventional research trial,
Beschreibung

Study Subject Participation Status | Interventional Study

Datentyp

boolean

Alias
UMLS CUI [1]
C2348568
UMLS CUI [2]
C3274035
unable to provide consent,
Beschreibung

infoInformed Consent Unable

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C1299582
asthma exacerbation within the last 4 weeks
Beschreibung

Exacerbation of asthma

Datentyp

boolean

Alias
UMLS CUI [1]
C0349790

Ähnliche Modelle

Eligibility Difficult Asthma NCT01862289

Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
C1512693 (UMLS CUI)
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])
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])
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])
Percent predicted FEV1
Item
forced expiratory volume in 1 second (fev1) > 50% predicted value
boolean
C0730561 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
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])
infoInformed Consent Unable
Item
unable to provide consent,
boolean
C0021430 (UMLS CUI [1,1])
C1299582 (UMLS CUI [1,2])
Exacerbation of asthma
Item
asthma exacerbation within the last 4 weeks
boolean
C0349790 (UMLS CUI [1])

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