ID

14375

Description

Persistence of Airway Inflammation and Remodeling in Subjects With Symptomatic or Complete Asthma Remission; ODM derived from: https://clinicaltrials.gov/show/NCT00526019

Link

https://clinicaltrials.gov/show/NCT00526019

Keywords

Versions (1)
  1. 4/12/16 4/12/16 -
Copyright Holder

CC BY-NC 3.0

Uploaded on

April 12, 2016

DOI

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License

Creative Commons BY-NC 3.0
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Eligibility Asthma NCT00526019

English

Eligibility Asthma NCT00526019

1 forms  
  1. StudyEvent: Eligibility
    1. Eligibility Asthma NCT00526019
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
in remission of their asthma: absence of respiratory symptoms, no rescue asthma medication need and (for complete remission) an optimal pulmonary function (fev1 > 90%) and normal pc20 methacholine for more than two years (with no current treatment).
Description

asthma remission

Data type

boolean

Alias
UMLS CUI [1,1]
C0004096
UMLS CUI [1,2]
C0544452
UMLS CUI [2]
C0748133
UMLS CUI [3]
C0430567
with a proven past history of asthma from medical files (reversible airway obstruction (> 12% fev1 after bronchodilator or 20% by other means) proven by spirometry, pef measures or methacholine challenge according to current criteria +
Description

history of asthma

Data type

boolean

Alias
UMLS CUI [1,1]
C0262926
UMLS CUI [1,2]
C0004096
UMLS CUI [2]
C0748133
UMLS CUI [3]
C0430567
UMLS CUI [4]
C0037981
UMLS CUI [5]
C0521299
previous symptoms and asthma medication use), having no more asthma symptoms and not having used asthma medication for more than 2 years.
Description

asthma symptoms and medication

Data type

boolean

Alias
UMLS CUI [1,1]
C0004096
UMLS CUI [1,2]
C1457887
UMLS CUI [2,1]
C0013227
UMLS CUI [2,2]
C0004096
UMLS CUI [2,3]
C0040223
agree to sign the consent form.
Description

agree to sign the consent form

Data type

boolean

Alias
UMLS CUI [1]
C0021430
no other condition that could interfere with the study measurements.
Description

comorbidity limiting study protocol

Data type

boolean

Alias
UMLS CUI [1,1]
C2348563
UMLS CUI [1,2]
C0439801
UMLS CUI [1,3]
C0009488
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
unable to adhere to the protocol requirements.
Description

compliance

Data type

boolean

Alias
UMLS CUI [1]
C1321605
other current respiratory disease.
Description

respiratory disease

Data type

boolean

Alias
UMLS CUI [1]
C0035204
upper or lower respiratory tract infection or use of antibiotics < 1 month.
Description

respiratory tract infection or antibiotics

Data type

boolean

Alias
UMLS CUI [1,1]
C0035243
UMLS CUI [1,2]
C0040223
UMLS CUI [2]
C0003232
use of oral corticosteroids within the last 3 months.
Description

use of oral corticosteroids

Data type

boolean

Alias
UMLS CUI [1]
C0001617
signs or symptoms of progressive or uncontrolled renal, hepatic, hematologic, endocrine, pulmonary, cardiac, neurologic, or cerebral disease.
Description

comorbidity

Data type

boolean

Alias
UMLS CUI [1]
C0009488
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Similar models

Eligibility Asthma NCT00526019

1 forms
  1. StudyEvent: Eligibility
    1. Eligibility Asthma NCT00526019
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
asthma remission
Item
in remission of their asthma: absence of respiratory symptoms, no rescue asthma medication need and (for complete remission) an optimal pulmonary function (fev1 > 90%) and normal pc20 methacholine for more than two years (with no current treatment).
boolean
C0004096 (UMLS CUI [1,1])
C0544452 (UMLS CUI [1,2])
C0748133 (UMLS CUI [2])
C0430567 (UMLS CUI [3])
history of asthma
Item
with a proven past history of asthma from medical files (reversible airway obstruction (> 12% fev1 after bronchodilator or 20% by other means) proven by spirometry, pef measures or methacholine challenge according to current criteria +
boolean
C0262926 (UMLS CUI [1,1])
C0004096 (UMLS CUI [1,2])
C0748133 (UMLS CUI [2])
C0430567 (UMLS CUI [3])
C0037981 (UMLS CUI [4])
C0521299 (UMLS CUI [5])
asthma symptoms and medication
Item
previous symptoms and asthma medication use), having no more asthma symptoms and not having used asthma medication for more than 2 years.
boolean
C0004096 (UMLS CUI [1,1])
C1457887 (UMLS CUI [1,2])
C0013227 (UMLS CUI [2,1])
C0004096 (UMLS CUI [2,2])
C0040223 (UMLS CUI [2,3])
agree to sign the consent form
Item
agree to sign the consent form.
boolean
C0021430 (UMLS CUI [1])
comorbidity limiting study protocol
Item
no other condition that could interfere with the study measurements.
boolean
C2348563 (UMLS CUI [1,1])
C0439801 (UMLS CUI [1,2])
C0009488 (UMLS CUI [1,3])
Item Group
C0680251 (UMLS CUI)
compliance
Item
unable to adhere to the protocol requirements.
boolean
C1321605 (UMLS CUI [1])
respiratory disease
Item
other current respiratory disease.
boolean
C0035204 (UMLS CUI [1])
respiratory tract infection or antibiotics
Item
upper or lower respiratory tract infection or use of antibiotics < 1 month.
boolean
C0035243 (UMLS CUI [1,1])
C0040223 (UMLS CUI [1,2])
C0003232 (UMLS CUI [2])
use of oral corticosteroids
Item
use of oral corticosteroids within the last 3 months.
boolean
C0001617 (UMLS CUI [1])
comorbidity
Item
signs or symptoms of progressive or uncontrolled renal, hepatic, hematologic, endocrine, pulmonary, cardiac, neurologic, or cerebral disease.
boolean
C0009488 (UMLS CUI [1])
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