ID

14500

Beskrivning

Oral Nadolol for the Treatment of Adults With Mild Asthma; ODM derived from: https://clinicaltrials.gov/show/NCT00670267

Länk

https://clinicaltrials.gov/show/NCT00670267

Nyckelord

  1. 2016-04-19 2016-04-19 -
Rättsinnehavare

CC BY-NC 3.0

Uppladdad den

19 april 2016

DOI

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Licens

Creative Commons BY-NC 3.0

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Eligibility Asthma NCT00670267

Eligibility Asthma NCT00670267

  1. StudyEvent: Eligibility
    1. Eligibility Asthma NCT00670267
Inclusion Criteria
Beskrivning

Inclusion Criteria

Alias
UMLS CUI
C1512693
pre-bronchodilator fev1 80% or greater than the predicted value.
Beskrivning

fev1 pre-bronchodilator

Datatyp

boolean

Alias
UMLS CUI [1]
C3172227
pc20 fev1 ≤4 mg/ml on methacholine challenge test.
Beskrivning

methacholine challenge fev1

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0430567
UMLS CUI [1,2]
C0748133
blood pressure ≥ 100/65mm hg.
Beskrivning

blood pressure

Datatyp

boolean

Alias
UMLS CUI [1]
C0005823
pulse rate ≥ 60 beats/min.
Beskrivning

pulse

Datatyp

boolean

Alias
UMLS CUI [1]
C0232117
no significant health issues.
Beskrivning

health status

Datatyp

boolean

Alias
UMLS CUI [1]
C0018759
non-smoker or x-smoker < 10 pack/year.
Beskrivning

smoking history

Datatyp

boolean

Alias
UMLS CUI [1]
C1519384
UMLS CUI [2]
C1277691
Exclusion Criteria
Beskrivning

Exclusion Criteria

Alias
UMLS CUI
C0680251
history of upper/lower respiratory tract infection or asthma exacerbation within 6 weeks of first baseline visit.
Beskrivning

asthma exacerbation or respiratory tract infection

Datatyp

boolean

Alias
UMLS CUI [1]
C0349790
UMLS CUI [2,1]
C0009450
UMLS CUI [2,2]
C0458827
UMLS CUI [3]
C0040223
currently diagnosed with chronic obstructive pulmonary disease (copd).
Beskrivning

copd

Datatyp

boolean

Alias
UMLS CUI [1]
C0024117
used any oral or inhaled corticosteroids within 4 weeks of the first baseline visit.
Beskrivning

oral or inhaled corticosteroids

Datatyp

boolean

Alias
UMLS CUI [1]
C2065041
UMLS CUI [2]
C0574135
UMLS CUI [3]
C0040223

Similar models

Eligibility Asthma NCT00670267

  1. StudyEvent: Eligibility
    1. Eligibility Asthma NCT00670267
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
C1512693 (UMLS CUI)
fev1 pre-bronchodilator
Item
pre-bronchodilator fev1 80% or greater than the predicted value.
boolean
C3172227 (UMLS CUI [1])
methacholine challenge fev1
Item
pc20 fev1 ≤4 mg/ml on methacholine challenge test.
boolean
C0430567 (UMLS CUI [1,1])
C0748133 (UMLS CUI [1,2])
blood pressure
Item
blood pressure ≥ 100/65mm hg.
boolean
C0005823 (UMLS CUI [1])
pulse
Item
pulse rate ≥ 60 beats/min.
boolean
C0232117 (UMLS CUI [1])
health status
Item
no significant health issues.
boolean
C0018759 (UMLS CUI [1])
smoking history
Item
non-smoker or x-smoker < 10 pack/year.
boolean
C1519384 (UMLS CUI [1])
C1277691 (UMLS CUI [2])
Item Group
C0680251 (UMLS CUI)
asthma exacerbation or respiratory tract infection
Item
history of upper/lower respiratory tract infection or asthma exacerbation within 6 weeks of first baseline visit.
boolean
C0349790 (UMLS CUI [1])
C0009450 (UMLS CUI [2,1])
C0458827 (UMLS CUI [2,2])
C0040223 (UMLS CUI [3])
copd
Item
currently diagnosed with chronic obstructive pulmonary disease (copd).
boolean
C0024117 (UMLS CUI [1])
oral or inhaled corticosteroids
Item
used any oral or inhaled corticosteroids within 4 weeks of the first baseline visit.
boolean
C2065041 (UMLS CUI [1])
C0574135 (UMLS CUI [2])
C0040223 (UMLS CUI [3])

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