ID

14369

Description

Efficacy of LAMA Added to ICS in Treatment of Asthma; ODM derived from: https://clinicaltrials.gov/show/NCT02296411

Lien

https://clinicaltrials.gov/show/NCT02296411

Mots-clés

  1. 12/04/2016 12/04/2016 -
Téléchargé le

12 avril 2016

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0

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Eligibility Asthma NCT02296411

Eligibility Asthma NCT02296411

  1. StudyEvent: Eligibility
    1. Eligibility Asthma NCT02296411
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
history of asthma ≥ 5 years and diagnosed before 40 years old
Description

Asthma | Age

Type de données

boolean

Alias
UMLS CUI [1]
C0004096
UMLS CUI [2]
C0001779
uncontrolled asthma on low-medium doses of inhaled corticosteroid (ics) with acq (asthma control questionnaire) ≥1.5
Description

Uncontrolled Asthma | inhaled steroids | Asthma control questionnaire

Type de données

boolean

Alias
UMLS CUI [1,1]
C0205318
UMLS CUI [1,2]
C0004096
UMLS CUI [2]
C2065041
UMLS CUI [3]
C2919686
pre-bronchodilator fev1 ≥40% and <90% of their predicted normal value
Description

FEV1 pre bronchodilator

Type de données

boolean

Alias
UMLS CUI [1,1]
C0748133
UMLS CUI [1,2]
C2599602
positive reversibility test
Description

Reversibility Test Result Positive

Type de données

boolean

Alias
UMLS CUI [1,1]
C0449261
UMLS CUI [1,2]
C0456984
UMLS CUI [1,3]
C1446409
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
pregnant or lactating women
Description

Pregnancy | Breast Feeding

Type de données

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
diagnosis of chronic obstructive pulmonary disease (copd)
Description

Chronic Obstructive Airway Disease

Type de données

boolean

Alias
UMLS CUI [1]
C0024117
patients treated for asthma exacerbation in the 4 weeks prior to study entry
Description

Therapeutic procedure Exacerbation of asthma

Type de données

boolean

Alias
UMLS CUI [1,1]
C0087111
UMLS CUI [1,2]
C0349790
patients who are in therapy for gastroesophageal reflux disease
Description

Therapeutic procedure Gastroesophageal reflux disease

Type de données

boolean

Alias
UMLS CUI [1,1]
C0087111
UMLS CUI [1,2]
C0017168
patients who have a clinically significant cardiovascular condition
Description

Cardiovascular Diseases

Type de données

boolean

Alias
UMLS CUI [1]
C0007222

Similar models

Eligibility Asthma NCT02296411

  1. StudyEvent: Eligibility
    1. Eligibility Asthma NCT02296411
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
C1512693 (UMLS CUI)
Asthma | Age
Item
history of asthma ≥ 5 years and diagnosed before 40 years old
boolean
C0004096 (UMLS CUI [1])
C0001779 (UMLS CUI [2])
Uncontrolled Asthma | inhaled steroids | Asthma control questionnaire
Item
uncontrolled asthma on low-medium doses of inhaled corticosteroid (ics) with acq (asthma control questionnaire) ≥1.5
boolean
C0205318 (UMLS CUI [1,1])
C0004096 (UMLS CUI [1,2])
C2065041 (UMLS CUI [2])
C2919686 (UMLS CUI [3])
FEV1 pre bronchodilator
Item
pre-bronchodilator fev1 ≥40% and <90% of their predicted normal value
boolean
C0748133 (UMLS CUI [1,1])
C2599602 (UMLS CUI [1,2])
Reversibility Test Result Positive
Item
positive reversibility test
boolean
C0449261 (UMLS CUI [1,1])
C0456984 (UMLS CUI [1,2])
C1446409 (UMLS CUI [1,3])
Item Group
C0680251 (UMLS CUI)
Pregnancy | Breast Feeding
Item
pregnant or lactating women
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Chronic Obstructive Airway Disease
Item
diagnosis of chronic obstructive pulmonary disease (copd)
boolean
C0024117 (UMLS CUI [1])
Therapeutic procedure Exacerbation of asthma
Item
patients treated for asthma exacerbation in the 4 weeks prior to study entry
boolean
C0087111 (UMLS CUI [1,1])
C0349790 (UMLS CUI [1,2])
Therapeutic procedure Gastroesophageal reflux disease
Item
patients who are in therapy for gastroesophageal reflux disease
boolean
C0087111 (UMLS CUI [1,1])
C0017168 (UMLS CUI [1,2])
Cardiovascular Diseases
Item
patients who have a clinically significant cardiovascular condition
boolean
C0007222 (UMLS CUI [1])

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