ID

14322

Beskrivning

A Comparative Study of Inhaled Ciclesonide Versus Placebo in Children With Asthma (6-11 y) (BY9010/M1-209); ODM derived from: https://clinicaltrials.gov/show/NCT00384189

Länk

https://clinicaltrials.gov/show/NCT00384189

Nyckelord

  1. 2016-04-11 2016-04-11 -
Rättsinnehavare

CC BY-NC 3.0

Uppladdad den

11 april 2016

DOI

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Licens

Creative Commons BY-NC 3.0

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Eligibility Asthma NCT00384189

Eligibility Asthma NCT00384189

  1. StudyEvent: Eligibility
    1. Eligibility Asthma NCT00384189
Criteria
Beskrivning

Criteria

history of asthma for at least 6 months
Beskrivning

history of asthma

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0262926
UMLS CUI [1,2]
C0004096
UMLS CUI [1,3]
C0040223
ability to show optimal use of mdi, including inhalation technique
Beskrivning

use of mdi

Datatyp

boolean

lung function and reversibility within specified limits
Beskrivning

lung function and reversibility

Datatyp

boolean

Alias
UMLS CUI [1]
C0024119
UMLS CUI [2]
C0679253
main exclusion criteria:
Beskrivning

exclusion criteria

Datatyp

boolean

Alias
UMLS CUI [1]
C0680251
concomitant severe diseases
Beskrivning

concomitant severe diseases

Datatyp

boolean

Alias
UMLS CUI [1]
C0009488
diseases which are contraindications for the use of inhaled steroids
Beskrivning

comorbidity limiting use of inhaled steroids

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0586793
UMLS CUI [1,2]
C0439801
UMLS CUI [1,3]
C0009488
two or more inpatient hospitalizations for asthma within the last year
Beskrivning

hospitalizations for asthma

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0019993
UMLS CUI [1,2]
C0004096
respiratory tract infection or asthma exacerbation within the last 30 days prior to entry into the study
Beskrivning

asthma exacerbation or respiratory tract infection

Datatyp

boolean

Alias
UMLS CUI [1]
C0349790
UMLS CUI [2,1]
C0009450
UMLS CUI [2,2]
C0458827
UMLS CUI [3]
C0040223
use of systemic steroids within the last 30 days prior to inclusion (depot steroids 6 weeks)
Beskrivning

systemic steroids

Datatyp

boolean

Alias
UMLS CUI [1]
C2825233
beginning of or change in immunotherapy within the last 6 months prior to inclusion
Beskrivning

immunotherapy

Datatyp

boolean

Alias
UMLS CUI [1]
C0021083
inability to follow the procedures of the study
Beskrivning

inability to follow the procedures of the study

Datatyp

boolean

Alias
UMLS CUI [1]
C1321605

Similar models

Eligibility Asthma NCT00384189

  1. StudyEvent: Eligibility
    1. Eligibility Asthma NCT00384189
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
history of asthma
Item
history of asthma for at least 6 months
boolean
C0262926 (UMLS CUI [1,1])
C0004096 (UMLS CUI [1,2])
C0040223 (UMLS CUI [1,3])
use of mdi
Item
ability to show optimal use of mdi, including inhalation technique
boolean
lung function and reversibility
Item
lung function and reversibility within specified limits
boolean
C0024119 (UMLS CUI [1])
C0679253 (UMLS CUI [2])
exclusion criteria
Item
main exclusion criteria:
boolean
C0680251 (UMLS CUI [1])
concomitant severe diseases
Item
concomitant severe diseases
boolean
C0009488 (UMLS CUI [1])
comorbidity limiting use of inhaled steroids
Item
diseases which are contraindications for the use of inhaled steroids
boolean
C0586793 (UMLS CUI [1,1])
C0439801 (UMLS CUI [1,2])
C0009488 (UMLS CUI [1,3])
hospitalizations for asthma
Item
two or more inpatient hospitalizations for asthma within the last year
boolean
C0019993 (UMLS CUI [1,1])
C0004096 (UMLS CUI [1,2])
asthma exacerbation or respiratory tract infection
Item
respiratory tract infection or asthma exacerbation within the last 30 days prior to entry into the study
boolean
C0349790 (UMLS CUI [1])
C0009450 (UMLS CUI [2,1])
C0458827 (UMLS CUI [2,2])
C0040223 (UMLS CUI [3])
systemic steroids
Item
use of systemic steroids within the last 30 days prior to inclusion (depot steroids 6 weeks)
boolean
C2825233 (UMLS CUI [1])
immunotherapy
Item
beginning of or change in immunotherapy within the last 6 months prior to inclusion
boolean
C0021083 (UMLS CUI [1])
inability to follow the procedures of the study
Item
inability to follow the procedures of the study
boolean
C1321605 (UMLS CUI [1])

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