ID

14187

Descripción

Trial of Asthma Patient Education (TAPE); ODM derived from: https://clinicaltrials.gov/show/NCT00148408

Link

https://clinicaltrials.gov/show/NCT00148408

Palabras clave

Versiones (1)
  1. 4/4/16 4/4/16 -
Titular de derechos de autor

CC BY-NC 3.0

Subido en

4 de abril de 2016

DOI

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Licencia

Creative Commons BY-NC 3.0
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Eligibility Asthma NCT00148408

Inglés

Eligibility Asthma NCT00148408

1 formularios  
  1. StudyEvent: Eligibility
    1. Eligibility Asthma NCT00148408
Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
age 15 or older
Descripción

age

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0001779
physician diagnosed asthma
Descripción

asthma

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0004096
regular use of prescribed asthma medication over preceding year
Descripción

asthma medication

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0013227
UMLS CUI [1,2]
C0004096
UMLS CUI [1,3]
C0040223
post-bronchodilator fev1 of at least 75% of predicted
Descripción

post-bronchodilator fev1

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0748133
UMLS CUI [1,2]
C2599594
inadequate asthma control over preceding two months
Descripción

asthma control

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0004096
UMLS CUI [1,2]
C0040223
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
current or past smoking (greater than 10 pack-years)
Descripción

smoking

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1519384
serious asthma exacerbation within previous three months
Descripción

asthma exacerbation

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0349790
UMLS CUI [1,2]
C0040223
regular use of oral corticosteroids
Descripción

oral corticosteroids

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0001617
history of respiratory failure due to asthma
Descripción

respiratory failure due to asthma

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C1145670
UMLS CUI [1,2]
C0004096
current use of montelukast or history of adverse reaction to montelukast
Descripción

montelukast

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0298130
UMLS CUI [2,1]
C0298130
UMLS CUI [2,2]
C0020517
concomitant interfering medical condition
Descripción

comorbidity

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0009488
participation in another clinical trial
Descripción

subject participation status

Tipo de datos

boolean

Alias
UMLS CUI [1]
C2348568
inability or unwillingness to perform study procedures
Descripción

compliance

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1321605
pregnancy, lack of effective contraception (when appropriate), lactation
Descripción

pregnancy, lack of effective contraception (when appropriate), lactation

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0700589
UMLS CUI [3]
C0006147
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Similar models

Eligibility Asthma NCT00148408

1 formularios
  1. StudyEvent: Eligibility
    1. Eligibility Asthma NCT00148408
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
age
Item
age 15 or older
boolean
C0001779 (UMLS CUI [1])
asthma
Item
physician diagnosed asthma
boolean
C0004096 (UMLS CUI [1])
asthma medication
Item
regular use of prescribed asthma medication over preceding year
boolean
C0013227 (UMLS CUI [1,1])
C0004096 (UMLS CUI [1,2])
C0040223 (UMLS CUI [1,3])
post-bronchodilator fev1
Item
post-bronchodilator fev1 of at least 75% of predicted
boolean
C0748133 (UMLS CUI [1,1])
C2599594 (UMLS CUI [1,2])
asthma control
Item
inadequate asthma control over preceding two months
boolean
C0004096 (UMLS CUI [1,1])
C0040223 (UMLS CUI [1,2])
Item Group
C0680251 (UMLS CUI)
smoking
Item
current or past smoking (greater than 10 pack-years)
boolean
C1519384 (UMLS CUI [1])
asthma exacerbation
Item
serious asthma exacerbation within previous three months
boolean
C0349790 (UMLS CUI [1,1])
C0040223 (UMLS CUI [1,2])
oral corticosteroids
Item
regular use of oral corticosteroids
boolean
C0001617 (UMLS CUI [1])
respiratory failure due to asthma
Item
history of respiratory failure due to asthma
boolean
C1145670 (UMLS CUI [1,1])
C0004096 (UMLS CUI [1,2])
montelukast
Item
current use of montelukast or history of adverse reaction to montelukast
boolean
C0298130 (UMLS CUI [1])
C0298130 (UMLS CUI [2,1])
C0020517 (UMLS CUI [2,2])
comorbidity
Item
concomitant interfering medical condition
boolean
C0009488 (UMLS CUI [1])
subject participation status
Item
participation in another clinical trial
boolean
C2348568 (UMLS CUI [1])
compliance
Item
inability or unwillingness to perform study procedures
boolean
C1321605 (UMLS CUI [1])
pregnancy, lack of effective contraception (when appropriate), lactation
Item
pregnancy, lack of effective contraception (when appropriate), lactation
boolean
C0032961 (UMLS CUI [1])
C0700589 (UMLS CUI [2])
C0006147 (UMLS CUI [3])
Volver a la parte superior de la página 

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