Eligibility Asthma NCT00453778

  1. StudyEvent: Eligibility
    1. Eligibility Asthma NCT00453778
Criteria
Descrizione

Criteria

diagnosed history of asthma
Descrizione

history of asthma

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0262926
UMLS CUI [1,2]
C0004096
non smoker last two years
Descrizione

non-smoker

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0337672
UMLS CUI [1,2]
C0040223
< 5 pack years
Descrizione

pack years

Tipo di dati

boolean

Alias
UMLS CUI [1]
C1277691
fev1 >70% of predicted
Descrizione

fev1

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0748133
mild and stable asthma
Descrizione

mild and stable asthma

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0741266
UMLS CUI [1,2]
C2945599
only using short acting b2-agonist as rescue for the last 4 weeks
Descrizione

short acting b2-agonist

Tipo di dati

boolean

Alias
UMLS CUI [1]
C1373132
have a history of atopy.
Descrizione

atopy

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0392707
exclusion:
Descrizione

exclusion

Tipo di dati

boolean

Alias
UMLS CUI [1]
C2828389
any significant respiratory disease, other than asthma
Descrizione

respiratory disease

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0035204
subjects with seasonal asthma may not be included if they are in their season
Descrizione

seasonal asthma

Tipo di dati

boolean

Alias
UMLS CUI [1]
C2919352
use of oral or inhaled glucocorticosteroid for the last 3 months and long-acting or oral b2-agonists, anticholinergic bronchodilators, cromones, antihistamines, theophyllines and antileukotrienes within two weeks
Descrizione

corticosteroids, b2-agonists, anticholinergic bronchodilators, cromones, antihistamines, theophyllines, antileukotrienes

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0001617
UMLS CUI [2]
C1373132
UMLS CUI [3]
C0039771
UMLS CUI [4]
C0354764
UMLS CUI [5]
C0019590
UMLS CUI [6]
C0595726
upper or lower rti within 6 weeks
Descrizione

respiratory tract infection

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0035243
UMLS CUI [1,2]
C0040223
evidence of any disease that in the investigators mind would affect the results of the study
Descrizione

comorbidity limiting study protocol

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C1321605
UMLS CUI [1,2]
C0439801
UMLS CUI [1,3]
C0009488
participating in another study within 4 weeks
Descrizione

participating in another study within 4 weeks

Tipo di dati

boolean

Alias
UMLS CUI [1]
C2348568
females who are pregnant, intend to be or who are lactating
Descrizione

pregnancy, lactation, intention to become pregnant

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2,1]
C0032961
UMLS CUI [2,2]
C1283828
UMLS CUI [3]
C0006147
methacholine pd20 > 454mcg
Descrizione

methacholine pd20

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0600370
negative scin prick test
Descrizione

skin prick test

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0430561

Similar models

Eligibility Asthma NCT00453778

  1. StudyEvent: Eligibility
    1. Eligibility Asthma NCT00453778
Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
Alias
Item Group
history of asthma
Item
diagnosed history of asthma
boolean
C0262926 (UMLS CUI [1,1])
C0004096 (UMLS CUI [1,2])
non-smoker
Item
non smoker last two years
boolean
C0337672 (UMLS CUI [1,1])
C0040223 (UMLS CUI [1,2])
pack years
Item
< 5 pack years
boolean
C1277691 (UMLS CUI [1])
fev1
Item
fev1 >70% of predicted
boolean
C0748133 (UMLS CUI [1])
mild and stable asthma
Item
mild and stable asthma
boolean
C0741266 (UMLS CUI [1,1])
C2945599 (UMLS CUI [1,2])
short acting b2-agonist
Item
only using short acting b2-agonist as rescue for the last 4 weeks
boolean
C1373132 (UMLS CUI [1])
atopy
Item
have a history of atopy.
boolean
C0392707 (UMLS CUI [1])
exclusion
Item
exclusion:
boolean
C2828389 (UMLS CUI [1])
respiratory disease
Item
any significant respiratory disease, other than asthma
boolean
C0035204 (UMLS CUI [1])
seasonal asthma
Item
subjects with seasonal asthma may not be included if they are in their season
boolean
C2919352 (UMLS CUI [1])
corticosteroids, b2-agonists, anticholinergic bronchodilators, cromones, antihistamines, theophyllines, antileukotrienes
Item
use of oral or inhaled glucocorticosteroid for the last 3 months and long-acting or oral b2-agonists, anticholinergic bronchodilators, cromones, antihistamines, theophyllines and antileukotrienes within two weeks
boolean
C0001617 (UMLS CUI [1])
C1373132 (UMLS CUI [2])
C0039771 (UMLS CUI [3])
C0354764 (UMLS CUI [4])
C0019590 (UMLS CUI [5])
C0595726 (UMLS CUI [6])
respiratory tract infection
Item
upper or lower rti within 6 weeks
boolean
C0035243 (UMLS CUI [1,1])
C0040223 (UMLS CUI [1,2])
comorbidity limiting study protocol
Item
evidence of any disease that in the investigators mind would affect the results of the study
boolean
C1321605 (UMLS CUI [1,1])
C0439801 (UMLS CUI [1,2])
C0009488 (UMLS CUI [1,3])
participating in another study within 4 weeks
Item
participating in another study within 4 weeks
boolean
C2348568 (UMLS CUI [1])
pregnancy, lactation, intention to become pregnant
Item
females who are pregnant, intend to be or who are lactating
boolean
C0032961 (UMLS CUI [1])
C0032961 (UMLS CUI [2,1])
C1283828 (UMLS CUI [2,2])
C0006147 (UMLS CUI [3])
methacholine pd20
Item
methacholine pd20 > 454mcg
boolean
C0600370 (UMLS CUI [1])
skin prick test
Item
negative scin prick test
boolean
C0430561 (UMLS CUI [1])