ID

14292

Description

A Comparative Study To Determine If Motivating Asthma Education (Compliance Enhancement) Has An Effect On Asthma Control; ODM derived from: https://clinicaltrials.gov/show/NCT00351143

Link

https://clinicaltrials.gov/show/NCT00351143

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 NCT00351143

English

Eligibility Asthma NCT00351143

1 forms  
  1. StudyEvent: Eligibility
    1. Eligibility Asthma NCT00351143
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
diagnosed with persistent asthma.
Description

persistent asthma

Data type

boolean

Alias
UMLS CUI [1]
C3266628
not treated with the combination of a ics (inhaled corticosteroid)and a laba (long-acting beta-agonist).
Description

ics and laba

Data type

boolean

Alias
UMLS CUI [1,1]
C3248292
UMLS CUI [1,2]
C0040223
UMLS CUI [2]
C2936789
female subjects must not be fertile or must use effective contraception.
Description

not be fertile or must use effective contraception

Data type

boolean

Alias
UMLS CUI [1]
C0021361
UMLS CUI [2]
C0700589
subject must be able to comply with the use of the questionnaires in the local language.
Description

compliance

Data type

boolean

Alias
UMLS CUI [1]
C1321605
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
known or suspected chronic obstructive pulmonary disease.
Description

copd

Data type

boolean

Alias
UMLS CUI [1]
C0024117
pregnant or lactating.
Description

pregnancy or lactation

Data type

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
participating investigator, employee of an investigator, or family member of any of the aforementioned.
Description

participating investigator, employee of an investigator, or family member of any of the aforementioned

Data type

boolean

smoking history: pack-years > 10 years.
Description

smoking history

Data type

boolean

Alias
UMLS CUI [1]
C1519384
UMLS CUI [2]
C1277691
have known clinical or laboratory evidence of a serious uncontrolled systemic disease.
Description

comorbidity

Data type

boolean

Alias
UMLS CUI [1]
C0009488
known hypersensitivity to any substance contained in investigational product or as-needed medication.
Description

hypersensitivity to investigational product

Data type

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C0013230
treatment with oral corticosteroid within 2 months prior to the screening visit.
Description

oral corticosteroid

Data type

boolean

Alias
UMLS CUI [1,1]
C0149783
UMLS CUI [1,2]
C0040223
upper or lower respiratory tract infection (microbiologically verified) within 1 month prior to screening visit.
Description

respiratory tract infection

Data type

boolean

Alias
UMLS CUI [1,1]
C0035243
UMLS CUI [1,2]
C0040223
acute asthma exacerbation requiring hospitalisation or emergency room treatment within 3 months prior to the screening visit.
Description

asthma exacerbation

Data type

boolean

Alias
UMLS CUI [1,1]
C0349790
UMLS CUI [1,2]
C0019993
UMLS CUI [2,1]
C0349790
UMLS CUI [2,2]
C0583237
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Similar models

Eligibility Asthma NCT00351143

1 forms
  1. StudyEvent: Eligibility
    1. Eligibility Asthma NCT00351143
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
persistent asthma
Item
diagnosed with persistent asthma.
boolean
C3266628 (UMLS CUI [1])
ics and laba
Item
not treated with the combination of a ics (inhaled corticosteroid)and a laba (long-acting beta-agonist).
boolean
C3248292 (UMLS CUI [1,1])
C0040223 (UMLS CUI [1,2])
C2936789 (UMLS CUI [2])
not be fertile or must use effective contraception
Item
female subjects must not be fertile or must use effective contraception.
boolean
C0021361 (UMLS CUI [1])
C0700589 (UMLS CUI [2])
compliance
Item
subject must be able to comply with the use of the questionnaires in the local language.
boolean
C1321605 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
copd
Item
known or suspected chronic obstructive pulmonary disease.
boolean
C0024117 (UMLS CUI [1])
pregnancy or lactation
Item
pregnant or lactating.
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
participating investigator, employee of an investigator, or family member of any of the aforementioned
Item
participating investigator, employee of an investigator, or family member of any of the aforementioned.
boolean
smoking history
Item
smoking history: pack-years > 10 years.
boolean
C1519384 (UMLS CUI [1])
C1277691 (UMLS CUI [2])
comorbidity
Item
have known clinical or laboratory evidence of a serious uncontrolled systemic disease.
boolean
C0009488 (UMLS CUI [1])
hypersensitivity to investigational product
Item
known hypersensitivity to any substance contained in investigational product or as-needed medication.
boolean
C0020517 (UMLS CUI [1,1])
C0013230 (UMLS CUI [1,2])
oral corticosteroid
Item
treatment with oral corticosteroid within 2 months prior to the screening visit.
boolean
C0149783 (UMLS CUI [1,1])
C0040223 (UMLS CUI [1,2])
respiratory tract infection
Item
upper or lower respiratory tract infection (microbiologically verified) within 1 month prior to screening visit.
boolean
C0035243 (UMLS CUI [1,1])
C0040223 (UMLS CUI [1,2])
asthma exacerbation
Item
acute asthma exacerbation requiring hospitalisation or emergency room treatment within 3 months prior to the screening visit.
boolean
C0349790 (UMLS CUI [1,1])
C0019993 (UMLS CUI [1,2])
C0349790 (UMLS CUI [2,1])
C0583237 (UMLS CUI [2,2])
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