Informations:
Erreur:
ID
35545
Description
Everolimus-eluting SYNERGY Stent Versus Biolimus-eluting Biomatrix NeoFlex Stent - SORT-OUT VIII; ODM derived from: https://clinicaltrials.gov/show/NCT02093845
Lien
https://clinicaltrials.gov/show/NCT02093845
Mots-clés
Versions (1)
- 08/03/2019 08/03/2019 -
Détendeur de droits
See clinicaltrials.gov
Téléchargé le
8 mars 2019
DOI
Pour une demande vous connecter.
Licence
Creative Commons BY 4.0
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Eligibility Coronary Artery Disease NCT02093845
Eligibility Coronary Artery Disease NCT02093845
- StudyEvent: Eligibility
Similar models
Eligibility Coronary Artery Disease NCT02093845
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Age | Patients Eligible Drug-Eluting Coronary Stents
Item
all patients aged ≥18 years who are eligible for treatment with one or several drug-eluting coronary stents at one of the three heart centers in odense, skejby and aalborg can be included in the study.
boolean
C0001779 (UMLS CUI [1])
C0030705 (UMLS CUI [2,1])
C1548635 (UMLS CUI [2,2])
C1262327 (UMLS CUI [2,3])
C0030705 (UMLS CUI [2,1])
C1548635 (UMLS CUI [2,2])
C1262327 (UMLS CUI [2,3])
Age
Item
age < 18 years
boolean
C0001779 (UMLS CUI [1])
Study Subject Participation Status Unwilling
Item
the patient does not wish to participate
boolean
C2348568 (UMLS CUI [1,1])
C0558080 (UMLS CUI [1,2])
C0558080 (UMLS CUI [1,2])
Randomization Consent Unable | Patients Intubation
Item
the patient is not able to consent to randomization (eg intubated patients)
boolean
C0034656 (UMLS CUI [1,1])
C1511481 (UMLS CUI [1,2])
C1299582 (UMLS CUI [1,3])
C0030705 (UMLS CUI [2,1])
C0021925 (UMLS CUI [2,2])
C1511481 (UMLS CUI [1,2])
C1299582 (UMLS CUI [1,3])
C0030705 (UMLS CUI [2,1])
C0021925 (UMLS CUI [2,2])
Patient Foreign National
Item
the patient do not live in west denmark
boolean
C0030705 (UMLS CUI [1,1])
C0870575 (UMLS CUI [1,2])
C0870575 (UMLS CUI [1,2])
Lacking Able to speak Danish language
Item
the patient do not speak danish
boolean
C0332268 (UMLS CUI [1,1])
C0564215 (UMLS CUI [1,2])
C0010969 (UMLS CUI [1,3])
C0564215 (UMLS CUI [1,2])
C0010969 (UMLS CUI [1,3])
Study Subject Participation Status
Item
the patient is already included in this study
boolean
C2348568 (UMLS CUI [1])
Study Subject Participation Status | Stent Clinical Trial
Item
the patient is already participating in other stent studies
boolean
C2348568 (UMLS CUI [1])
C0038257 (UMLS CUI [2,1])
C0008976 (UMLS CUI [2,2])
C0038257 (UMLS CUI [2,1])
C0008976 (UMLS CUI [2,2])
Life Expectancy
Item
life expectancy <1 year
boolean
C0023671 (UMLS CUI [1])
Aspirin allergy | Hypersensitivity Clopidogrel | Hypersensitivity Prasugrel | Hypersensitivity Ticagrelor
Item
allergic to aspirin, clopidogrel, prasugrel or ticagrelor
boolean
C0004058 (UMLS CUI [1])
C0020517 (UMLS CUI [2,1])
C0070166 (UMLS CUI [2,2])
C0020517 (UMLS CUI [3,1])
C1620287 (UMLS CUI [3,2])
C0020517 (UMLS CUI [4,1])
C1999375 (UMLS CUI [4,2])
C0020517 (UMLS CUI [2,1])
C0070166 (UMLS CUI [2,2])
C0020517 (UMLS CUI [3,1])
C1620287 (UMLS CUI [3,2])
C0020517 (UMLS CUI [4,1])
C1999375 (UMLS CUI [4,2])
Hypersensitivity Everolimus | Hypersensitivity Biolimus A9
Item
allergic to everolimus or biolimus
boolean
C0020517 (UMLS CUI [1,1])
C0541315 (UMLS CUI [1,2])
C0020517 (UMLS CUI [2,1])
C4310325 (UMLS CUI [2,2])
C0541315 (UMLS CUI [1,2])
C0020517 (UMLS CUI [2,1])
C4310325 (UMLS CUI [2,2])
Bare metal stent implanted only
Item
only implanted bms
boolean
C2825200 (UMLS CUI [1,1])
C0021102 (UMLS CUI [1,2])
C0205171 (UMLS CUI [1,3])
C0021102 (UMLS CUI [1,2])
C0205171 (UMLS CUI [1,3])
Other Coding
Item
only performed poba
boolean
C3846158 (UMLS CUI [1])