ID

14375

Beschreibung

Persistence of Airway Inflammation and Remodeling in Subjects With Symptomatic or Complete Asthma Remission; ODM derived from: https://clinicaltrials.gov/show/NCT00526019

Link

https://clinicaltrials.gov/show/NCT00526019

Stichworte

  1. 12.04.16 12.04.16 -
Rechteinhaber

CC BY-NC 3.0

Hochgeladen am

12. 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 :


Keine Kommentare

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

Eligibility Asthma NCT00526019

Eligibility Asthma NCT00526019

  1. StudyEvent: Eligibility
    1. Eligibility Asthma NCT00526019
Inclusion Criteria
Beschreibung

Inclusion Criteria

Alias
UMLS CUI
C1512693
in remission of their asthma: absence of respiratory symptoms, no rescue asthma medication need and (for complete remission) an optimal pulmonary function (fev1 > 90%) and normal pc20 methacholine for more than two years (with no current treatment).
Beschreibung

asthma remission

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0004096
UMLS CUI [1,2]
C0544452
UMLS CUI [2]
C0748133
UMLS CUI [3]
C0430567
with a proven past history of asthma from medical files (reversible airway obstruction (> 12% fev1 after bronchodilator or 20% by other means) proven by spirometry, pef measures or methacholine challenge according to current criteria +
Beschreibung

history of asthma

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0262926
UMLS CUI [1,2]
C0004096
UMLS CUI [2]
C0748133
UMLS CUI [3]
C0430567
UMLS CUI [4]
C0037981
UMLS CUI [5]
C0521299
previous symptoms and asthma medication use), having no more asthma symptoms and not having used asthma medication for more than 2 years.
Beschreibung

asthma symptoms and medication

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0004096
UMLS CUI [1,2]
C1457887
UMLS CUI [2,1]
C0013227
UMLS CUI [2,2]
C0004096
UMLS CUI [2,3]
C0040223
agree to sign the consent form.
Beschreibung

agree to sign the consent form

Datentyp

boolean

Alias
UMLS CUI [1]
C0021430
no other condition that could interfere with the study measurements.
Beschreibung

comorbidity limiting study protocol

Datentyp

boolean

Alias
UMLS CUI [1,1]
C2348563
UMLS CUI [1,2]
C0439801
UMLS CUI [1,3]
C0009488
Exclusion Criteria
Beschreibung

Exclusion Criteria

Alias
UMLS CUI
C0680251
unable to adhere to the protocol requirements.
Beschreibung

compliance

Datentyp

boolean

Alias
UMLS CUI [1]
C1321605
other current respiratory disease.
Beschreibung

respiratory disease

Datentyp

boolean

Alias
UMLS CUI [1]
C0035204
upper or lower respiratory tract infection or use of antibiotics < 1 month.
Beschreibung

respiratory tract infection or antibiotics

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0035243
UMLS CUI [1,2]
C0040223
UMLS CUI [2]
C0003232
use of oral corticosteroids within the last 3 months.
Beschreibung

use of oral corticosteroids

Datentyp

boolean

Alias
UMLS CUI [1]
C0001617
signs or symptoms of progressive or uncontrolled renal, hepatic, hematologic, endocrine, pulmonary, cardiac, neurologic, or cerebral disease.
Beschreibung

comorbidity

Datentyp

boolean

Alias
UMLS CUI [1]
C0009488

Ähnliche Modelle

Eligibility Asthma NCT00526019

  1. StudyEvent: Eligibility
    1. Eligibility Asthma NCT00526019
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
C1512693 (UMLS CUI)
asthma remission
Item
in remission of their asthma: absence of respiratory symptoms, no rescue asthma medication need and (for complete remission) an optimal pulmonary function (fev1 > 90%) and normal pc20 methacholine for more than two years (with no current treatment).
boolean
C0004096 (UMLS CUI [1,1])
C0544452 (UMLS CUI [1,2])
C0748133 (UMLS CUI [2])
C0430567 (UMLS CUI [3])
history of asthma
Item
with a proven past history of asthma from medical files (reversible airway obstruction (> 12% fev1 after bronchodilator or 20% by other means) proven by spirometry, pef measures or methacholine challenge according to current criteria +
boolean
C0262926 (UMLS CUI [1,1])
C0004096 (UMLS CUI [1,2])
C0748133 (UMLS CUI [2])
C0430567 (UMLS CUI [3])
C0037981 (UMLS CUI [4])
C0521299 (UMLS CUI [5])
asthma symptoms and medication
Item
previous symptoms and asthma medication use), having no more asthma symptoms and not having used asthma medication for more than 2 years.
boolean
C0004096 (UMLS CUI [1,1])
C1457887 (UMLS CUI [1,2])
C0013227 (UMLS CUI [2,1])
C0004096 (UMLS CUI [2,2])
C0040223 (UMLS CUI [2,3])
agree to sign the consent form
Item
agree to sign the consent form.
boolean
C0021430 (UMLS CUI [1])
comorbidity limiting study protocol
Item
no other condition that could interfere with the study measurements.
boolean
C2348563 (UMLS CUI [1,1])
C0439801 (UMLS CUI [1,2])
C0009488 (UMLS CUI [1,3])
Item Group
C0680251 (UMLS CUI)
compliance
Item
unable to adhere to the protocol requirements.
boolean
C1321605 (UMLS CUI [1])
respiratory disease
Item
other current respiratory disease.
boolean
C0035204 (UMLS CUI [1])
respiratory tract infection or antibiotics
Item
upper or lower respiratory tract infection or use of antibiotics < 1 month.
boolean
C0035243 (UMLS CUI [1,1])
C0040223 (UMLS CUI [1,2])
C0003232 (UMLS CUI [2])
use of oral corticosteroids
Item
use of oral corticosteroids within the last 3 months.
boolean
C0001617 (UMLS CUI [1])
comorbidity
Item
signs or symptoms of progressive or uncontrolled renal, hepatic, hematologic, endocrine, pulmonary, cardiac, neurologic, or cerebral disease.
boolean
C0009488 (UMLS CUI [1])

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