ID

14251

Beschreibung

Effect of an Inhaled Corticosteroid on Airway Gene Expression in Asthma; ODM derived from: https://clinicaltrials.gov/show/NCT00187499

Link

https://clinicaltrials.gov/show/NCT00187499

Stichworte

  1. 05.04.16 05.04.16 -
Rechteinhaber

CC BY-NC 3.0

Hochgeladen am

5. April 2016

DOI

Für eine Beantragung loggen Sie sich ein.

Lizenz

Creative Commons BY-NC 3.0

Modell Kommentare :

Hier können Sie das Modell kommentieren. Über die Sprechblasen an den Itemgruppen und Items können Sie diese spezifisch kommentieren.

Itemgroup Kommentare für :

Item Kommentare für :

Um Formulare herunterzuladen müssen Sie angemeldet sein. Bitte loggen Sie sich ein oder registrieren Sie sich kostenlos.

Eligibility Asthma NCT00187499

Eligibility Asthma NCT00187499

  1. StudyEvent: Eligibility
    1. Eligibility Asthma NCT00187499
Inclusion Criteria
Beschreibung

Inclusion Criteria

Alias
UMLS CUI
C1512693
male and female patients with a history of asthma between the ages of 18 and 70 years.
Beschreibung

asthma and age

Datentyp

boolean

Alias
UMLS CUI [1]
C0004096
UMLS CUI [2]
C0001779
pc20fev1 methacholine ≤ 8.0 mg/ml.
Beschreibung

pc20fev1 methacholine

Datentyp

boolean

Alias
UMLS CUI [1]
C1714620
at least one of the following symptoms, beta agonist use, or fev1 criteria:
Beschreibung

ID.3

Datentyp

boolean

asthma symptoms on at least two days per week or beta agonist use on at least two days per week or fev1 < 85% predicted
Beschreibung

asthma symptoms

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0004096
UMLS CUI [1,2]
C1457887
UMLS CUI [2]
C0001644
UMLS CUI [3]
C0748133
subjects must be non-smokers (patients who have never smoked or patients who have not smoked for 1 year and have a total pack-year smoking history < 15 packs).
Beschreibung

non-smoker

Datentyp

boolean

Alias
UMLS CUI [1]
C0337672
Exclusion Criteria
Beschreibung

Exclusion Criteria

Alias
UMLS CUI
C0680251
history of oral or inhaled steroid use in the past 4 weeks.
Beschreibung

steroid

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0038317
UMLS CUI [1,2]
C0040223
fev1 < 60% predicted.
Beschreibung

fev1

Datentyp

boolean

Alias
UMLS CUI [1]
C0748133
lung disease other than asthma.
Beschreibung

lung disease

Datentyp

boolean

Alias
UMLS CUI [1]
C0024115
patients with a history of a respiratory tract infection in the 4 weeks preceding the study.
Beschreibung

respiratory tract infection

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0035243
UMLS CUI [1,2]
C0040223
patients who have experienced a significant exacerbation in their asthma in the 6 weeks prior to the study.
Beschreibung

asthma exacerbation

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0349790
UMLS CUI [1,2]
C0040223
patients receiving hyposensitization therapy with the exception of those who are on a stable dose for the last three months.
Beschreibung

hyposensitization

Datentyp

boolean

Alias
UMLS CUI [1]
C0178702
patients with cardiovascular disease (active) peptic ulcer disease or diabetes mellitus.
Beschreibung

cardiovascular disease, peptic ulcer diseases or diabetes mellitus

Datentyp

boolean

Alias
UMLS CUI [1]
C0007222
UMLS CUI [2]
C0030920
UMLS CUI [3]
C0011849
females who are lactating or who are pregnant.
Beschreibung

pregnancy or lactation

Datentyp

boolean

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

Ähnliche Modelle

Eligibility Asthma NCT00187499

  1. StudyEvent: Eligibility
    1. Eligibility Asthma NCT00187499
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
C1512693 (UMLS CUI)
asthma and age
Item
male and female patients with a history of asthma between the ages of 18 and 70 years.
boolean
C0004096 (UMLS CUI [1])
C0001779 (UMLS CUI [2])
pc20fev1 methacholine
Item
pc20fev1 methacholine ≤ 8.0 mg/ml.
boolean
C1714620 (UMLS CUI [1])
ID.3
Item
at least one of the following symptoms, beta agonist use, or fev1 criteria:
boolean
asthma symptoms
Item
asthma symptoms on at least two days per week or beta agonist use on at least two days per week or fev1 < 85% predicted
boolean
C0004096 (UMLS CUI [1,1])
C1457887 (UMLS CUI [1,2])
C0001644 (UMLS CUI [2])
C0748133 (UMLS CUI [3])
non-smoker
Item
subjects must be non-smokers (patients who have never smoked or patients who have not smoked for 1 year and have a total pack-year smoking history < 15 packs).
boolean
C0337672 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
steroid
Item
history of oral or inhaled steroid use in the past 4 weeks.
boolean
C0038317 (UMLS CUI [1,1])
C0040223 (UMLS CUI [1,2])
fev1
Item
fev1 < 60% predicted.
boolean
C0748133 (UMLS CUI [1])
lung disease
Item
lung disease other than asthma.
boolean
C0024115 (UMLS CUI [1])
respiratory tract infection
Item
patients with a history of a respiratory tract infection in the 4 weeks preceding the study.
boolean
C0035243 (UMLS CUI [1,1])
C0040223 (UMLS CUI [1,2])
asthma exacerbation
Item
patients who have experienced a significant exacerbation in their asthma in the 6 weeks prior to the study.
boolean
C0349790 (UMLS CUI [1,1])
C0040223 (UMLS CUI [1,2])
hyposensitization
Item
patients receiving hyposensitization therapy with the exception of those who are on a stable dose for the last three months.
boolean
C0178702 (UMLS CUI [1])
cardiovascular disease, peptic ulcer diseases or diabetes mellitus
Item
patients with cardiovascular disease (active) peptic ulcer disease or diabetes mellitus.
boolean
C0007222 (UMLS CUI [1])
C0030920 (UMLS CUI [2])
C0011849 (UMLS CUI [3])
pregnancy or lactation
Item
females who are lactating or who are pregnant.
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])

Benutzen Sie dieses Formular für Rückmeldungen, Fragen und Verbesserungsvorschläge.

Mit * gekennzeichnete Felder sind notwendig.

Benötigen Sie Hilfe bei der Suche? Um mehr Details zu erfahren und die Suche effektiver nutzen zu können schauen Sie sich doch das entsprechende Video auf unserer Tutorial Seite an.

Zum Video