ID

14286

Descripción

Responsiveness of Lower Airways in Adult Patients (18-60 Years) With Stable Asthma After Treatment With Ciclesonide and Fluticasone Propionate (BY9010/NL-101); ODM derived from: https://clinicaltrials.gov/show/NCT00306163

Link

https://clinicaltrials.gov/show/NCT00306163

Palabras clave

  1. 7/4/16 7/4/16 -
Titular de derechos de autor

CC BY-NC 3.0

Subido en

7 de abril de 2016

DOI

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Licencia

Creative Commons BY-NC 3.0

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Eligibility Asthma NCT00306163

Eligibility Asthma NCT00306163

  1. StudyEvent: Eligibility
    1. Eligibility Asthma NCT00306163
Criteria
Descripción

Criteria

history of bronchial asthma
Descripción

history of bronchial asthma

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0004096
fev1 > 1.20 l
Descripción

fev1

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0748133
positive skin prick test
Descripción

positive skin prick test

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0430561
not more than 500 mcg/day fluticasone propionate or equivalent for at least 28 days prior to baseline visit
Descripción

fluticasone propionate

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0117996
UMLS CUI [1,2]
C0040223
main exclusion criteria:
Descripción

exclusion criteria

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0680251
clinically relevant abnormal laboratory values
Descripción

clinically relevant abnormal laboratory values

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C1254595
UMLS CUI [1,2]
C2826293
concomitant severe diseases, diseases expected to interfere with the outcome of the study and diseases which are contra-indications for the use of inhaled steroids
Descripción

concomitant severe diseases, diseases expected to interfere with the outcome of the study and diseases which are contra-indications for the use of inhaled steroids

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C1321605
UMLS CUI [1,2]
C0439801
UMLS CUI [1,3]
C0009488
UMLS CUI [2,1]
C0586793
UMLS CUI [2,2]
C0439801
UMLS CUI [2,3]
C0009488
chronic obstructive pulmonary disease (copd) and /or other relevant lung diseases
Descripción

copd or other relevant lung diseases

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0024117
UMLS CUI [1,2]
C0024115
one asthma exacerbation within 2 months or more than 3 exacerbations within the last year prior to baseline visit
Descripción

asthma exacerbation

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0349790
UMLS CUI [1,2]
C0040223
current smokers or ex-smokers with more than 10 pack years, or having smoked within 1 year prior to baseline visit
Descripción

smoking history

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1519384
UMLS CUI [2]
C1277691
positive response to saline challenge at baseline visits
Descripción

saline challenge

Tipo de datos

boolean

positive bronchial hyperresponsiveness
Descripción

bronchial hyperresponsiveness

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0085129

Similar models

Eligibility Asthma NCT00306163

  1. StudyEvent: Eligibility
    1. Eligibility Asthma NCT00306163
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
history of bronchial asthma
Item
history of bronchial asthma
boolean
C0004096 (UMLS CUI [1])
fev1
Item
fev1 > 1.20 l
boolean
C0748133 (UMLS CUI [1])
positive skin prick test
Item
positive skin prick test
boolean
C0430561 (UMLS CUI [1])
fluticasone propionate
Item
not more than 500 mcg/day fluticasone propionate or equivalent for at least 28 days prior to baseline visit
boolean
C0117996 (UMLS CUI [1,1])
C0040223 (UMLS CUI [1,2])
exclusion criteria
Item
main exclusion criteria:
boolean
C0680251 (UMLS CUI [1])
clinically relevant abnormal laboratory values
Item
clinically relevant abnormal laboratory values
boolean
C1254595 (UMLS CUI [1,1])
C2826293 (UMLS CUI [1,2])
concomitant severe diseases, diseases expected to interfere with the outcome of the study and diseases which are contra-indications for the use of inhaled steroids
Item
concomitant severe diseases, diseases expected to interfere with the outcome of the study and diseases which are contra-indications for the use of inhaled steroids
boolean
C1321605 (UMLS CUI [1,1])
C0439801 (UMLS CUI [1,2])
C0009488 (UMLS CUI [1,3])
C0586793 (UMLS CUI [2,1])
C0439801 (UMLS CUI [2,2])
C0009488 (UMLS CUI [2,3])
copd or other relevant lung diseases
Item
chronic obstructive pulmonary disease (copd) and /or other relevant lung diseases
boolean
C0024117 (UMLS CUI [1,1])
C0024115 (UMLS CUI [1,2])
asthma exacerbation
Item
one asthma exacerbation within 2 months or more than 3 exacerbations within the last year prior to baseline visit
boolean
C0349790 (UMLS CUI [1,1])
C0040223 (UMLS CUI [1,2])
smoking history
Item
current smokers or ex-smokers with more than 10 pack years, or having smoked within 1 year prior to baseline visit
boolean
C1519384 (UMLS CUI [1])
C1277691 (UMLS CUI [2])
saline challenge
Item
positive response to saline challenge at baseline visits
boolean
bronchial hyperresponsiveness
Item
positive bronchial hyperresponsiveness
boolean
C0085129 (UMLS CUI [1])

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