ID

14278

Descripción

Airway Hyper-responsiveness Study In Asthma Using Salmeterol/Fluticasone Propionate Combination Product; ODM derived from: https://clinicaltrials.gov/show/NCT00291382

Link

https://clinicaltrials.gov/show/NCT00291382

Palabras clave

Versiones (1)
  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

Para solicitar uno, por favor iniciar sesión.

Licencia

Creative Commons BY-NC 3.0
Comentarios del modelo :

Puede comentar sobre el modelo de datos aquí. A través de las burbujas de diálogo en los grupos de elementos y elementos, puede agregar comentarios específicos.

Volver a los comentarios del modelo
Comentarios de grupo de elementos para :

Comentarios del elemento para :

Para descargar modelos de datos, debe haber iniciado sesión. Por favor iniciar sesión o Registrate gratis.

Eligibility Asthma NCT00291382

Inglés

Eligibility Asthma NCT00291382

1 formularios  
  1. StudyEvent: Eligibility
    1. Eligibility Asthma NCT00291382
Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
history of asthma of at least 6 months.
Descripción

history of asthma

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0262926
UMLS CUI [1,2]
C0004096
UMLS CUI [1,3]
C0040223
subjects who have received fluticasone propionate at a dose of 100 mcg bd to 250 mcg bd or equivalent with or without a long acting beta2-agonist for at least 4 weeks before the start of the run-in period, at a constant dose.
Descripción

fluticasone propionate

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0117996
UMLS CUI [2]
C2936789
subjects who are able to understand and complete an electronic diary card.
Descripción

able to understand and complete an electronic diary card

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1321605
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
subjects who have been hospitalized for their asthma within 4 weeks of study entry.
Descripción

hospitalization

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0019993
UMLS CUI [1,2]
C0040223
subjects who had an acute upper respiratory tract infection within 4 weeks or a lower respiratory tract infection within 4 weeks prior to study entry.
Descripción

respiratory tract infection

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0035243
UMLS CUI [1,2]
C0040223
subjects who received oral, parental or depot corticosteroids within 4 weeks prior to study entry.
Descripción

corticosteroids

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0001617
UMLS CUI [1,2]
C0040223
subjects who have a known respiratory disorder other than asthma and/or systemic/thoracic abnormalities which influence normal lung function.
Descripción

respiratory disorders or other abnormalities influencing normal lung function

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0035204
UMLS CUI [2,1]
C0024119
UMLS CUI [2,2]
C0439801
UMLS CUI [2,3]
C0009488
subjects who have more than 5 pack years.
Descripción

pack years

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1277691
subjects who currently smoke.
Descripción

current smoker

Tipo de datos

boolean

Alias
UMLS CUI [1]
C3241966
Volver a la parte superior de la página

Similar models

Eligibility Asthma NCT00291382

1 formularios
  1. StudyEvent: Eligibility
    1. Eligibility Asthma NCT00291382
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
history of asthma
Item
history of asthma of at least 6 months.
boolean
C0262926 (UMLS CUI [1,1])
C0004096 (UMLS CUI [1,2])
C0040223 (UMLS CUI [1,3])
fluticasone propionate
Item
subjects who have received fluticasone propionate at a dose of 100 mcg bd to 250 mcg bd or equivalent with or without a long acting beta2-agonist for at least 4 weeks before the start of the run-in period, at a constant dose.
boolean
C0117996 (UMLS CUI [1])
C2936789 (UMLS CUI [2])
able to understand and complete an electronic diary card
Item
subjects who are able to understand and complete an electronic diary card.
boolean
C1321605 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
hospitalization
Item
subjects who have been hospitalized for their asthma within 4 weeks of study entry.
boolean
C0019993 (UMLS CUI [1,1])
C0040223 (UMLS CUI [1,2])
respiratory tract infection
Item
subjects who had an acute upper respiratory tract infection within 4 weeks or a lower respiratory tract infection within 4 weeks prior to study entry.
boolean
C0035243 (UMLS CUI [1,1])
C0040223 (UMLS CUI [1,2])
corticosteroids
Item
subjects who received oral, parental or depot corticosteroids within 4 weeks prior to study entry.
boolean
C0001617 (UMLS CUI [1,1])
C0040223 (UMLS CUI [1,2])
respiratory disorders or other abnormalities influencing normal lung function
Item
subjects who have a known respiratory disorder other than asthma and/or systemic/thoracic abnormalities which influence normal lung function.
boolean
C0035204 (UMLS CUI [1])
C0024119 (UMLS CUI [2,1])
C0439801 (UMLS CUI [2,2])
C0009488 (UMLS CUI [2,3])
pack years
Item
subjects who have more than 5 pack years.
boolean
C1277691 (UMLS CUI [1])
current smoker
Item
subjects who currently smoke.
boolean
C3241966 (UMLS CUI [1])
Volver a la parte superior de la página 

Contacto

Utilice este formulario para comentarios, preguntas y sugerencias.

Los campos marcados con * son obligatorios.

Ayuda

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial