ID

17241

Beskrivning

Obesity and Asthma:a Specific Phenotype; ODM derived from: https://clinicaltrials.gov/show/NCT00532363

Länk

https://clinicaltrials.gov/show/NCT00532363

Nyckelord

  1. 2016-09-01 2016-09-01 -
Uppladdad den

1 september 2016

DOI

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Licens

Creative Commons BY 4.0

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Eligibility Obesity NCT00532363

Eligibility Obesity NCT00532363

  1. StudyEvent: Eligibility
    1. Eligibility Obesity NCT00532363
Inclusion Criteria
Beskrivning

Inclusion Criteria

Alias
UMLS CUI
C1512693
will be women aged 18 years and over
Beskrivning

Gender, Age

Datatyp

boolean

Alias
UMLS CUI [1]
C0079399
UMLS CUI [2]
C0001779
will be in good health apart from asthma or obesity as determined by history and physical examination (no other condition that could influence the proposed tests).
Beskrivning

Good health as determined by history and physical examination

Datatyp

boolean

Alias
UMLS CUI [1]
C0018759
UMLS CUI [2]
C0031809
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.)
Beskrivning

non smokers or ex-smokers for more than six months

Datatyp

boolean

Alias
UMLS CUI [1]
C0543414
subjects will have a physician's made diagnosis of severe asthma and treated with corticosteroids.
Beskrivning

severe asthma treated with corticosteroids

Datatyp

boolean

Alias
UMLS CUI [1]
C0581126
UMLS CUI [2]
C0001617
Exclusion Criteria
Beskrivning

Exclusion Criteria

Alias
UMLS CUI
C0680251
subjects who are, in the opinion of the investigator, mentally or legally incapacitated thus preventing informed consent from being obtained.
Beskrivning

Informed consent

Datatyp

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.
Beskrivning

Comorbidity

Datatyp

boolean

Alias
UMLS CUI [1,1]
C1321605
UMLS CUI [1,2]
C0439801
UMLS CUI [1,3]
C0009488
pregnancy or lactation
Beskrivning

Pregnancy or lactation

Datatyp

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
contraindication to the prednisone treatment.
Beskrivning

Contraindication to prednisone treatment

Datatyp

boolean

Alias
UMLS CUI [1,1]
C1301624
UMLS CUI [1,2]
C0032952

Similar models

Eligibility Obesity NCT00532363

  1. StudyEvent: Eligibility
    1. Eligibility Obesity NCT00532363
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
C1512693 (UMLS CUI)
Gender, Age
Item
will be women aged 18 years and over
boolean
C0079399 (UMLS CUI [1])
C0001779 (UMLS CUI [2])
Good health as determined by history and physical examination
Item
will be in good health apart from asthma or obesity as determined by history and physical examination (no other condition that could influence the proposed tests).
boolean
C0018759 (UMLS CUI [1])
C0031809 (UMLS CUI [2])
non smokers or ex-smokers for more than six months
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
C0543414 (UMLS CUI [1])
severe asthma treated with corticosteroids
Item
subjects will have a physician's made diagnosis of severe asthma and treated with corticosteroids.
boolean
C0581126 (UMLS CUI [1])
C0001617 (UMLS CUI [2])
Item Group
C0680251 (UMLS CUI)
Informed consent
Item
subjects who are, in the opinion of the investigator, mentally or legally 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
Item
subjects having a co-existing illness that precludes them from the trial.
boolean
C1321605 (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])
Contraindication to prednisone treatment
Item
contraindication to the prednisone treatment.
boolean
C1301624 (UMLS CUI [1,1])
C0032952 (UMLS CUI [1,2])

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