ID

14395

Beschrijving

Characterisation of Asthma in Obese Subjects; ODM derived from: https://clinicaltrials.gov/show/NCT00532831

Link

https://clinicaltrials.gov/show/NCT00532831

Trefwoorden

Versies (1)
  1. 13-04-16 13-04-16 -
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CC BY-NC 3.0

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13 april 2016

DOI

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Licentie

Creative Commons BY-NC 3.0
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Eligibility Asthma NCT00532831

Engels

Eligibility Asthma NCT00532831

1 Formulieren  
  1. StudyEvent: Eligibility
    1. Eligibility Asthma NCT00532831
Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
aged 18 and over.
Beschrijving

age

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
in good health apart from asthma or obesity as determined by history and physical examination (no other condition which could influence the proposed tests).
Beschrijving

good health apart from asthma or obesity as determined by history and physical examination

Datatype

boolean

Alias
UMLS CUI [1,1]
C0018759
UMLS CUI [1,2]
C0205170
UMLS CUI [2]
C0031809
UMLS CUI [3]
C0028754
UMLS CUI [4]
C0004096
all will be non smokers or ex- smokers for more than six months with a smoking history of no more than 10 pack- years (i.e., one pack per day or its equivalent for 10 years.)
Beschrijving

smoking history

Datatype

boolean

Alias
UMLS CUI [1]
C1519384
UMLS CUI [2]
C1277691
UMLS CUI [3]
C0337672
UMLS CUI [4]
C0040223
subjects will have a physician's made diagnosis of asthma and have received a bronchodilator prescription in the last year.
Beschrijving

asthma and bronchodilator

Datatype

boolean

Alias
UMLS CUI [1]
C0004096
UMLS CUI [2]
C0040223
UMLS CUI [3]
C0006280
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
use of asthma medications other than bronchodilators
Beschrijving

asthma medications other than bronchodilators

Datatype

boolean

Alias
UMLS CUI [1,1]
C0013227
UMLS CUI [1,2]
C0004096
UMLS CUI [2]
C0006280
subjects who are, in the opinion of the investigator, mentally or legally
Beschrijving

ID.6

Datatype

boolean

incapacitated thus preventing informed consent from being obtained.
Beschrijving

limited informed consent

Datatype

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C0439801
UMLS CUI [1,3]
C0009488
subjects having a co-existing illness that precludes them from the trial.
Beschrijving

comorbidity limiting study protocol

Datatype

boolean

Alias
UMLS CUI [1,1]
C2348563
UMLS CUI [1,2]
C0439801
UMLS CUI [1,3]
C0009488
pregnancy or lactation
Beschrijving

pregnancy or lactation

Datatype

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
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Similar models

Eligibility Asthma NCT00532831

1 Formulieren
  1. StudyEvent: Eligibility
    1. Eligibility Asthma NCT00532831
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
age
Item
aged 18 and over.
boolean
C0001779 (UMLS CUI [1])
good health apart from asthma or obesity as determined by history and physical examination
Item
in good health apart from asthma or obesity as determined by history and physical examination (no other condition which could influence the proposed tests).
boolean
C0018759 (UMLS CUI [1,1])
C0205170 (UMLS CUI [1,2])
C0031809 (UMLS CUI [2])
C0028754 (UMLS CUI [3])
C0004096 (UMLS CUI [4])
smoking history
Item
all will be non smokers or ex- smokers for more than six months with a smoking history of no more than 10 pack- years (i.e., one pack per day or its equivalent for 10 years.)
boolean
C1519384 (UMLS CUI [1])
C1277691 (UMLS CUI [2])
C0337672 (UMLS CUI [3])
C0040223 (UMLS CUI [4])
asthma and bronchodilator
Item
subjects will have a physician's made diagnosis of asthma and have received a bronchodilator prescription in the last year.
boolean
C0004096 (UMLS CUI [1])
C0040223 (UMLS CUI [2])
C0006280 (UMLS CUI [3])
Item Group
C0680251 (UMLS CUI)
asthma medications other than bronchodilators
Item
use of asthma medications other than bronchodilators
boolean
C0013227 (UMLS CUI [1,1])
C0004096 (UMLS CUI [1,2])
C0006280 (UMLS CUI [2])
ID.6
Item
subjects who are, in the opinion of the investigator, mentally or legally
boolean
limited informed consent
Item
incapacitated thus preventing informed consent from being obtained.
boolean
C0021430 (UMLS CUI [1,1])
C0439801 (UMLS CUI [1,2])
C0009488 (UMLS CUI [1,3])
comorbidity limiting study protocol
Item
subjects having a co-existing illness that precludes them from the trial.
boolean
C2348563 (UMLS CUI [1,1])
C0439801 (UMLS CUI [1,2])
C0009488 (UMLS CUI [1,3])
pregnancy or lactation
Item
pregnancy or lactation
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
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