ID

14149

Description

Asthma Biomarkers for Predicting Response to Therapy; ODM derived from: https://clinicaltrials.gov/show/NCT01973751

Link

https://clinicaltrials.gov/show/NCT01973751

Keywords

  1. 4/1/16 4/1/16 -
Uploaded on

April 1, 2016

DOI

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License

Creative Commons BY 4.0

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Eligibility Asthma NCT01973751

Eligibility Asthma NCT01973751

  1. StudyEvent: Eligibility
    1. Eligibility Asthma NCT01973751
Criteria
Description

Criteria

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
male and female subjects between the ages of 18 and 70 years
Description

Age | Gender

Data type

boolean

Alias
UMLS CUI [1,1]
C0001779
UMLS CUI [1,2]
C0079399
no respiratory symptoms
Description

No respiratory symptoms

Data type

boolean

Alias
UMLS CUI [1]
C0425443
normal spirometric value and methacholine pd20 >2.5mg
Description

Spirometry normal | Methacholine

Data type

boolean

Alias
UMLS CUI [1]
C0855776
UMLS CUI [2]
C0600370
group b:
Description

ID.4

Data type

boolean

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
male and female subjects between the ages of 18 and 70 years
Description

Age | Gender

Data type

boolean

Alias
UMLS CUI [1]
C0001779
UMLS CUI [2]
C0079399
history of asthma
Description

Asthma

Data type

boolean

Alias
UMLS CUI [1]
C0004096
no use of oral or inhaled corticosteroids for the treatment of asthma
Description

Therapeutic procedure | Asthma | Adrenal Cortex Hormones | inhaled steroids

Data type

boolean

Alias
UMLS CUI [1,1]
C0087111
UMLS CUI [1,2]
C0004096
UMLS CUI [2]
C0001617
UMLS CUI [3]
C2065041
no use of leukotriene antagonist for the treatment of asthma
Description

Therapeutic procedure | Asthma | Leukotriene Antagonists

Data type

boolean

Alias
UMLS CUI [1,1]
C0087111
UMLS CUI [1,2]
C0004096
UMLS CUI [2]
C0595726
hyperreactivity to methacholine (pd20 fev1 methacholine < 2.5 mg) and/or ≥12% increase in fev1 following inhalation of 200μg salbutamol
Description

Pulmonary methacholine challenge test | FEV1 | Albuterol

Data type

boolean

Alias
UMLS CUI [1]
C1096470
UMLS CUI [2]
C0748133
UMLS CUI [3]
C0001927
asthma symptoms of episodic cough, wheeze and/or breathlessness
Description

Asthma symptoms | Coughing | Rhonchi | Dyspnea

Data type

boolean

Alias
UMLS CUI [1,1]
C0004096
UMLS CUI [1,2]
C1457887
UMLS CUI [2]
C0010200
UMLS CUI [3]
C0035508
UMLS CUI [4]
C0013404
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
current or former smokers
Description

Current Smoker | Former smoker

Data type

boolean

Alias
UMLS CUI [1]
C3241966
UMLS CUI [2]
C0337671
pregnant women
Description

Pregnancy

Data type

boolean

Alias
UMLS CUI [1]
C0032961
subjects with a history of lung disease other than asthma
Description

Lung disease

Data type

boolean

Alias
UMLS CUI [1]
C0024115
UMLS CUI [2]
C0004096
subjects with a history of a medical disease, which in the opinion of the investigator may put the subject at extra risk from study-related procedures or because the disease may influence the results of the study
Description

Disease | Study Subject Participation Status

Data type

boolean

Alias
UMLS CUI [1]
C0012634
UMLS CUI [2]
C2348568

Similar models

Eligibility Asthma NCT01973751

  1. StudyEvent: Eligibility
    1. Eligibility Asthma NCT01973751
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Item Group
C1512693 (UMLS CUI)
Age | Gender
Item
male and female subjects between the ages of 18 and 70 years
boolean
C0001779 (UMLS CUI [1,1])
C0079399 (UMLS CUI [1,2])
No respiratory symptoms
Item
no respiratory symptoms
boolean
C0425443 (UMLS CUI [1])
Spirometry normal | Methacholine
Item
normal spirometric value and methacholine pd20 >2.5mg
boolean
C0855776 (UMLS CUI [1])
C0600370 (UMLS CUI [2])
ID.4
Item
group b:
boolean
Item Group
C1512693 (UMLS CUI)
Age | Gender
Item
male and female subjects between the ages of 18 and 70 years
boolean
C0001779 (UMLS CUI [1])
C0079399 (UMLS CUI [2])
Asthma
Item
history of asthma
boolean
C0004096 (UMLS CUI [1])
Therapeutic procedure | Asthma | Adrenal Cortex Hormones | inhaled steroids
Item
no use of oral or inhaled corticosteroids for the treatment of asthma
boolean
C0087111 (UMLS CUI [1,1])
C0004096 (UMLS CUI [1,2])
C0001617 (UMLS CUI [2])
C2065041 (UMLS CUI [3])
Therapeutic procedure | Asthma | Leukotriene Antagonists
Item
no use of leukotriene antagonist for the treatment of asthma
boolean
C0087111 (UMLS CUI [1,1])
C0004096 (UMLS CUI [1,2])
C0595726 (UMLS CUI [2])
Pulmonary methacholine challenge test | FEV1 | Albuterol
Item
hyperreactivity to methacholine (pd20 fev1 methacholine < 2.5 mg) and/or ≥12% increase in fev1 following inhalation of 200μg salbutamol
boolean
C1096470 (UMLS CUI [1])
C0748133 (UMLS CUI [2])
C0001927 (UMLS CUI [3])
Asthma symptoms | Coughing | Rhonchi | Dyspnea
Item
asthma symptoms of episodic cough, wheeze and/or breathlessness
boolean
C0004096 (UMLS CUI [1,1])
C1457887 (UMLS CUI [1,2])
C0010200 (UMLS CUI [2])
C0035508 (UMLS CUI [3])
C0013404 (UMLS CUI [4])
Item Group
C0680251 (UMLS CUI)
Current Smoker | Former smoker
Item
current or former smokers
boolean
C3241966 (UMLS CUI [1])
C0337671 (UMLS CUI [2])
Pregnancy
Item
pregnant women
boolean
C0032961 (UMLS CUI [1])
Lung disease
Item
subjects with a history of lung disease other than asthma
boolean
C0024115 (UMLS CUI [1])
C0004096 (UMLS CUI [2])
Disease | Study Subject Participation Status
Item
subjects with a history of a medical disease, which in the opinion of the investigator may put the subject at extra risk from study-related procedures or because the disease may influence the results of the study
boolean
C0012634 (UMLS CUI [1])
C2348568 (UMLS CUI [2])

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