Informatie:
Fout:
ID
14292
Beschrijving
A Comparative Study To Determine If Motivating Asthma Education (Compliance Enhancement) Has An Effect On Asthma Control; ODM derived from: https://clinicaltrials.gov/show/NCT00351143
Link
https://clinicaltrials.gov/show/NCT00351143
Trefwoorden
Versies (1)
- 07-04-16 07-04-16 -
Houder van rechten
CC BY-NC 3.0
Geüploaded op
7 april 2016
DOI
Voor een aanvraag inloggen.
Licentie
Creative Commons BY-NC 3.0
Model Commentaren :
Hier kunt u commentaar leveren op het model. U kunt de tekstballonnen bij de itemgroepen en items gebruiken om er specifiek commentaar op te geven.
Itemgroep Commentaren voor :
Item Commentaren voor :
U moet ingelogd zijn om formulieren te downloaden. AUB inloggen of schrijf u gratis in.
Eligibility Asthma NCT00351143
Eligibility Asthma NCT00351143
- StudyEvent: Eligibility
Similar models
Eligibility Asthma NCT00351143
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
persistent asthma
Item
diagnosed with persistent asthma.
boolean
C3266628 (UMLS CUI [1])
ics and laba
Item
not treated with the combination of a ics (inhaled corticosteroid)and a laba (long-acting beta-agonist).
boolean
C3248292 (UMLS CUI [1,1])
C0040223 (UMLS CUI [1,2])
C2936789 (UMLS CUI [2])
C0040223 (UMLS CUI [1,2])
C2936789 (UMLS CUI [2])
not be fertile or must use effective contraception
Item
female subjects must not be fertile or must use effective contraception.
boolean
C0021361 (UMLS CUI [1])
C0700589 (UMLS CUI [2])
C0700589 (UMLS CUI [2])
compliance
Item
subject must be able to comply with the use of the questionnaires in the local language.
boolean
C1321605 (UMLS CUI [1])
copd
Item
known or suspected chronic obstructive pulmonary disease.
boolean
C0024117 (UMLS CUI [1])
pregnancy or lactation
Item
pregnant or lactating.
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C0006147 (UMLS CUI [2])
participating investigator, employee of an investigator, or family member of any of the aforementioned
Item
participating investigator, employee of an investigator, or family member of any of the aforementioned.
boolean
smoking history
Item
smoking history: pack-years > 10 years.
boolean
C1519384 (UMLS CUI [1])
C1277691 (UMLS CUI [2])
C1277691 (UMLS CUI [2])
comorbidity
Item
have known clinical or laboratory evidence of a serious uncontrolled systemic disease.
boolean
C0009488 (UMLS CUI [1])
hypersensitivity to investigational product
Item
known hypersensitivity to any substance contained in investigational product or as-needed medication.
boolean
C0020517 (UMLS CUI [1,1])
C0013230 (UMLS CUI [1,2])
C0013230 (UMLS CUI [1,2])
oral corticosteroid
Item
treatment with oral corticosteroid within 2 months prior to the screening visit.
boolean
C0149783 (UMLS CUI [1,1])
C0040223 (UMLS CUI [1,2])
C0040223 (UMLS CUI [1,2])
respiratory tract infection
Item
upper or lower respiratory tract infection (microbiologically verified) within 1 month prior to screening visit.
boolean
C0035243 (UMLS CUI [1,1])
C0040223 (UMLS CUI [1,2])
C0040223 (UMLS CUI [1,2])
asthma exacerbation
Item
acute asthma exacerbation requiring hospitalisation or emergency room treatment within 3 months prior to the screening visit.
boolean
C0349790 (UMLS CUI [1,1])
C0019993 (UMLS CUI [1,2])
C0349790 (UMLS CUI [2,1])
C0583237 (UMLS CUI [2,2])
C0019993 (UMLS CUI [1,2])
C0349790 (UMLS CUI [2,1])
C0583237 (UMLS CUI [2,2])