ID

14199

Beschreibung

Efficacy of Ciclesonide and Fluticasone Propionate in Adult Patients With Moderate and Severe Persistent Asthma (18 to 75 y) (BY9010/IT-101); ODM derived from: https://clinicaltrials.gov/show/NCT00163319

Link

https://clinicaltrials.gov/show/NCT00163319

Stichworte

  1. 04.04.16 04.04.16 -
  2. 05.04.16 05.04.16 -
Rechteinhaber

CC BY-NC 3.0

Hochgeladen am

4. April 2016

DOI

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Lizenz

Creative Commons BY-NC 3.0

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Eligibility Asthma NCT00163319

Eligibility Asthma NCT00163319

  1. StudyEvent: Eligibility
    1. Eligibility Asthma NCT00163319
Criteria
Beschreibung

Criteria

written informed consent
Beschreibung

written informed consent

Datentyp

boolean

Alias
UMLS CUI [1]
C0021430
history of bronchial asthma for at least 6 months
Beschreibung

asthma

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0004096
UMLS CUI [1,2]
C0040223
pre-treatment with cfc-beclomethasone dipropionate (cfc-bdp) ≥ 1000 mcg/day or equivalent and a long-acting beta agonist (laba) either in free or fixed combination
Beschreibung

cfc-beclomethasone dipropionate and a long-acting beta agonist

Datentyp

boolean

Alias
UMLS CUI [1]
C0004906
UMLS CUI [2]
C2936789
fev1 ≥ 80% of predicted
Beschreibung

fev1

Datentyp

boolean

Alias
UMLS CUI [1]
C0748133
main exclusion criteria:
Beschreibung

ID.5

Datentyp

boolean

concomitant severe diseases or diseases which are contraindications for the use of inhaled steroids or contraindications for the use of labas
Beschreibung

comorbidity limiting inhaled steroids

Datentyp

boolean

Alias
UMLS CUI [1,1]
C2065041
UMLS CUI [1,2]
C0439801
UMLS CUI [1,3]
C0009488
UMLS CUI [2,1]
C2936789
UMLS CUI [2,2]
C0439801
UMLS CUI [2,3]
C0009488
copd
Beschreibung

copd

Datentyp

boolean

Alias
UMLS CUI [1]
C0024117
smoking with ≥10 pack-years
Beschreibung

pack years

Datentyp

boolean

Alias
UMLS CUI [1]
C1277691
pregnancy
Beschreibung

pregnancy

Datentyp

boolean

Alias
UMLS CUI [1]
C0032961
intention to become pregnant during the course of the study
Beschreibung

intention to become pregnant

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0032961
UMLS CUI [1,2]
C1283828
breast feeding
Beschreibung

lactation

Datentyp

boolean

Alias
UMLS CUI [1]
C0006147
lack of safe contraception
Beschreibung

contraception

Datentyp

boolean

Alias
UMLS CUI [1]
C0700589

Ähnliche Modelle

Eligibility Asthma NCT00163319

  1. StudyEvent: Eligibility
    1. Eligibility Asthma NCT00163319
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
written informed consent
Item
written informed consent
boolean
C0021430 (UMLS CUI [1])
asthma
Item
history of bronchial asthma for at least 6 months
boolean
C0004096 (UMLS CUI [1,1])
C0040223 (UMLS CUI [1,2])
cfc-beclomethasone dipropionate and a long-acting beta agonist
Item
pre-treatment with cfc-beclomethasone dipropionate (cfc-bdp) ≥ 1000 mcg/day or equivalent and a long-acting beta agonist (laba) either in free or fixed combination
boolean
C0004906 (UMLS CUI [1])
C2936789 (UMLS CUI [2])
fev1
Item
fev1 ≥ 80% of predicted
boolean
C0748133 (UMLS CUI [1])
ID.5
Item
main exclusion criteria:
boolean
comorbidity limiting inhaled steroids
Item
concomitant severe diseases or diseases which are contraindications for the use of inhaled steroids or contraindications for the use of labas
boolean
C2065041 (UMLS CUI [1,1])
C0439801 (UMLS CUI [1,2])
C0009488 (UMLS CUI [1,3])
C2936789 (UMLS CUI [2,1])
C0439801 (UMLS CUI [2,2])
C0009488 (UMLS CUI [2,3])
copd
Item
copd
boolean
C0024117 (UMLS CUI [1])
pack years
Item
smoking with ≥10 pack-years
boolean
C1277691 (UMLS CUI [1])
pregnancy
Item
pregnancy
boolean
C0032961 (UMLS CUI [1])
intention to become pregnant
Item
intention to become pregnant during the course of the study
boolean
C0032961 (UMLS CUI [1,1])
C1283828 (UMLS CUI [1,2])
lactation
Item
breast feeding
boolean
C0006147 (UMLS CUI [1])
contraception
Item
lack of safe contraception
boolean
C0700589 (UMLS CUI [1])

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