ID

40455

Beschrijving

The Long-term Prognosis of Moderate to Severe Bronchial Hyperresponsiveness (BHR) in Asthmatic Preschool Children; ODM derived from: https://clinicaltrials.gov/show/NCT01144910

Link

https://clinicaltrials.gov/show/NCT01144910

Trefwoorden

Versies (1)
  1. 23-04-20 23-04-20 -
Houder van rechten

See clinicaltrials.gov

Geüploaded op

23 april 2020

DOI

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Licentie

Creative Commons BY 4.0
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Eligibility Intrinsic Asthma NCT01144910

Engels

Eligibility Intrinsic Asthma NCT01144910

1 Formulieren  
Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
informed consent
Beschrijving

Informed Consent

Datatype

boolean

Alias
UMLS CUI [1]
C0021430
age 3 to 6 years
Beschrijving

Age

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
diagnosis asthma
Beschrijving

Asthma

Datatype

boolean

Alias
UMLS CUI [1]
C0004096
pulmonary function: fev1 (% pred.)≥ 70%
Beschrijving

Pulmonary function | Percent predicted FEV1

Datatype

boolean

Alias
UMLS CUI [1]
C0231921
UMLS CUI [2]
C0730561
ability to carry out 2 reproducible flow volume loops
Beschrijving

Ability Flow volume loop Quantity

Datatype

boolean

Alias
UMLS CUI [1,1]
C0085732
UMLS CUI [1,2]
C0428734
UMLS CUI [1,3]
C1265611
moderate to severe bhr (pd20 fev1 ≤ 0,3 mg methacholine)
Beschrijving

Bronchial Hyperreactivity Moderate | Bronchial Hyperreactivity Severe | FEV1 Methacholine

Datatype

boolean

Alias
UMLS CUI [1,1]
C0085129
UMLS CUI [1,2]
C0205081
UMLS CUI [2,1]
C0085129
UMLS CUI [2,2]
C0205082
UMLS CUI [3,1]
C0849974
UMLS CUI [3,2]
C0600370
more than 4 weeks interval since last infection
Beschrijving

Interval Since Communicable Disease

Datatype

boolean

Alias
UMLS CUI [1,1]
C1272706
UMLS CUI [1,2]
C1711239
UMLS CUI [1,3]
C0009450
8 hours washout period of short acting beta agonist
Beschrijving

Washout Period Adrenergic beta-Agonists Active short-term

Datatype

boolean

Alias
UMLS CUI [1,1]
C1710661
UMLS CUI [1,2]
C0001644
UMLS CUI [1,3]
C0205177
UMLS CUI [1,4]
C0443303
1 week washout period of ipratropium bromide
Beschrijving

Washout Period Ipratropium Bromide

Datatype

boolean

Alias
UMLS CUI [1,1]
C1710661
UMLS CUI [1,2]
C0700580
1 week washout period of long acting beta agonist
Beschrijving

Washout Period Adrenergic beta-Agonists Active Long-term

Datatype

boolean

Alias
UMLS CUI [1,1]
C1710661
UMLS CUI [1,2]
C0001644
UMLS CUI [1,3]
C0205177
UMLS CUI [1,4]
C0443252
4 weeks washout period of systemic corticosteroids
Beschrijving

Washout Period CORTICOSTEROIDS FOR SYSTEMIC USE

Datatype

boolean

Alias
UMLS CUI [1,1]
C1710661
UMLS CUI [1,2]
C3653708
4 weeks washout period of leukotriene antagonists
Beschrijving

Washout Period Leukotriene Antagonists

Datatype

boolean

Alias
UMLS CUI [1,1]
C1710661
UMLS CUI [1,2]
C0595726
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
age < 3 and > 6 years
Beschrijving

Age

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
pulmonary function test: fev1 (% pred.) < 70%
Beschrijving

Pulmonary function test | Percent predicted FEV1

Datatype

boolean

Alias
UMLS CUI [1]
C0024119
UMLS CUI [2]
C0730561
others chronic diseases or infections (e.g., hiv, tuberculosis, malignancy)
Beschrijving

Chronic disease | Chronic infectious disease | HIV Infection | Tuberculosis | Malignant Neoplasms

Datatype

boolean

Alias
UMLS CUI [1]
C0008679
UMLS CUI [2]
C0151317
UMLS CUI [3]
C0019693
UMLS CUI [4]
C0041296
UMLS CUI [5]
C0006826
incapability to perform spirometry
Beschrijving

Spirometry Perform Unable

Datatype

boolean

Alias
UMLS CUI [1,1]
C0037981
UMLS CUI [1,2]
C0884358
UMLS CUI [1,3]
C1299582
current participation in another clinical trial
Beschrijving

Study Subject Participation Status | Clinical Trial

Datatype

boolean

Alias
UMLS CUI [1]
C2348568
UMLS CUI [2]
C0008976
Terug naar het begin van de pagina

Similar models

Eligibility Intrinsic Asthma NCT01144910

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
Informed Consent
Item
informed consent
boolean
C0021430 (UMLS CUI [1])
Age
Item
age 3 to 6 years
boolean
C0001779 (UMLS CUI [1])
Asthma
Item
diagnosis asthma
boolean
C0004096 (UMLS CUI [1])
Pulmonary function | Percent predicted FEV1
Item
pulmonary function: fev1 (% pred.)≥ 70%
boolean
C0231921 (UMLS CUI [1])
C0730561 (UMLS CUI [2])
Ability Flow volume loop Quantity
Item
ability to carry out 2 reproducible flow volume loops
boolean
C0085732 (UMLS CUI [1,1])
C0428734 (UMLS CUI [1,2])
C1265611 (UMLS CUI [1,3])
Bronchial Hyperreactivity Moderate | Bronchial Hyperreactivity Severe | FEV1 Methacholine
Item
moderate to severe bhr (pd20 fev1 ≤ 0,3 mg methacholine)
boolean
C0085129 (UMLS CUI [1,1])
C0205081 (UMLS CUI [1,2])
C0085129 (UMLS CUI [2,1])
C0205082 (UMLS CUI [2,2])
C0849974 (UMLS CUI [3,1])
C0600370 (UMLS CUI [3,2])
Interval Since Communicable Disease
Item
more than 4 weeks interval since last infection
boolean
C1272706 (UMLS CUI [1,1])
C1711239 (UMLS CUI [1,2])
C0009450 (UMLS CUI [1,3])
Washout Period Adrenergic beta-Agonists Active short-term
Item
8 hours washout period of short acting beta agonist
boolean
C1710661 (UMLS CUI [1,1])
C0001644 (UMLS CUI [1,2])
C0205177 (UMLS CUI [1,3])
C0443303 (UMLS CUI [1,4])
Washout Period Ipratropium Bromide
Item
1 week washout period of ipratropium bromide
boolean
C1710661 (UMLS CUI [1,1])
C0700580 (UMLS CUI [1,2])
Washout Period Adrenergic beta-Agonists Active Long-term
Item
1 week washout period of long acting beta agonist
boolean
C1710661 (UMLS CUI [1,1])
C0001644 (UMLS CUI [1,2])
C0205177 (UMLS CUI [1,3])
C0443252 (UMLS CUI [1,4])
Washout Period CORTICOSTEROIDS FOR SYSTEMIC USE
Item
4 weeks washout period of systemic corticosteroids
boolean
C1710661 (UMLS CUI [1,1])
C3653708 (UMLS CUI [1,2])
Washout Period Leukotriene Antagonists
Item
4 weeks washout period of leukotriene antagonists
boolean
C1710661 (UMLS CUI [1,1])
C0595726 (UMLS CUI [1,2])
Item Group
C0680251 (UMLS CUI)
Age
Item
age < 3 and > 6 years
boolean
C0001779 (UMLS CUI [1])
Pulmonary function test | Percent predicted FEV1
Item
pulmonary function test: fev1 (% pred.) < 70%
boolean
C0024119 (UMLS CUI [1])
C0730561 (UMLS CUI [2])
Chronic disease | Chronic infectious disease | HIV Infection | Tuberculosis | Malignant Neoplasms
Item
others chronic diseases or infections (e.g., hiv, tuberculosis, malignancy)
boolean
C0008679 (UMLS CUI [1])
C0151317 (UMLS CUI [2])
C0019693 (UMLS CUI [3])
C0041296 (UMLS CUI [4])
C0006826 (UMLS CUI [5])
Spirometry Perform Unable
Item
incapability to perform spirometry
boolean
C0037981 (UMLS CUI [1,1])
C0884358 (UMLS CUI [1,2])
C1299582 (UMLS CUI [1,3])
Study Subject Participation Status | Clinical Trial
Item
current participation in another clinical trial
boolean
C2348568 (UMLS CUI [1])
C0008976 (UMLS CUI [2])
Terug naar het begin van de pagina 

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