ID

14519

Description

Repeated High-dose Inhaled Corticosteroids for Asthma; ODM derived from: https://clinicaltrials.gov/show/NCT00695604

Lien

https://clinicaltrials.gov/show/NCT00695604

Mots-clés

  1. 19/04/2016 19/04/2016 -
Détendeur de droits

CC BY-NC 3.0

Téléchargé le

19 avril 2016

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY-NC 3.0

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Eligibility Asthma NCT00695604

Eligibility Asthma NCT00695604

  1. StudyEvent: Eligibility
    1. Eligibility Asthma NCT00695604
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
physician diagnosis of asthma.
Description

asthma

Type de données

boolean

Alias
UMLS CUI [1]
C0004096
age ≥18 years and ≤50 years
Description

age

Type de données

boolean

Alias
UMLS CUI [1]
C0001779
evidence of airflow obstruction as measured by spirometry and flow-volume loop per american thoracic society guidelines.
Description

airflow obstruction

Type de données

boolean

Alias
UMLS CUI [1]
C1527303
UMLS CUI [2]
C0037981
treatment for asthma with:
Description

asthma therapy

Type de données

boolean

Alias
UMLS CUI [1,1]
C0087111
UMLS CUI [1,2]
C0004096
daily inhaled corticosteroids and long-acting beta2-agonists, and
Description

inhaled corticosteroids and long-acting beta2-agonists

Type de données

boolean

Alias
UMLS CUI [1]
C2065041
UMLS CUI [2]
C1373132
as-needed use of a short-acting beta2-agonist
Description

short-acting beta2-agonist

Type de données

boolean

Alias
UMLS CUI [1]
C1373132
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
history of >10 pack-year tobacco use
Description

smoking history

Type de données

boolean

Alias
UMLS CUI [1]
C1519384
UMLS CUI [2]
C1277691
other pulmonary or cardiac diagnosis that is actively being treated
Description

comorbidity

Type de données

boolean

Alias
UMLS CUI [1]
C0009488
history of adverse events or allergy to fluticasone
Description

adverse events or allergy to fluticasone

Type de données

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C0082607
systemic corticosteroid therapy within 7 days of study visit
Description

systemic steroid therapy

Type de données

boolean

Alias
UMLS CUI [1,1]
C4039704
UMLS CUI [1,2]
C0040223
inability to obtain written informed consent
Description

inability to obtain written informed consent

Type de données

boolean

Alias
UMLS CUI [1]
C0021430

Similar models

Eligibility Asthma NCT00695604

  1. StudyEvent: Eligibility
    1. Eligibility Asthma NCT00695604
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
C1512693 (UMLS CUI)
asthma
Item
physician diagnosis of asthma.
boolean
C0004096 (UMLS CUI [1])
age
Item
age ≥18 years and ≤50 years
boolean
C0001779 (UMLS CUI [1])
airflow obstruction
Item
evidence of airflow obstruction as measured by spirometry and flow-volume loop per american thoracic society guidelines.
boolean
C1527303 (UMLS CUI [1])
C0037981 (UMLS CUI [2])
asthma therapy
Item
treatment for asthma with:
boolean
C0087111 (UMLS CUI [1,1])
C0004096 (UMLS CUI [1,2])
inhaled corticosteroids and long-acting beta2-agonists
Item
daily inhaled corticosteroids and long-acting beta2-agonists, and
boolean
C2065041 (UMLS CUI [1])
C1373132 (UMLS CUI [2])
short-acting beta2-agonist
Item
as-needed use of a short-acting beta2-agonist
boolean
C1373132 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
smoking history
Item
history of >10 pack-year tobacco use
boolean
C1519384 (UMLS CUI [1])
C1277691 (UMLS CUI [2])
comorbidity
Item
other pulmonary or cardiac diagnosis that is actively being treated
boolean
C0009488 (UMLS CUI [1])
adverse events or allergy to fluticasone
Item
history of adverse events or allergy to fluticasone
boolean
C0020517 (UMLS CUI [1,1])
C0082607 (UMLS CUI [1,2])
systemic steroid therapy
Item
systemic corticosteroid therapy within 7 days of study visit
boolean
C4039704 (UMLS CUI [1,1])
C0040223 (UMLS CUI [1,2])
inability to obtain written informed consent
Item
inability to obtain written informed consent
boolean
C0021430 (UMLS CUI [1])

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