Informationen:
Fehler:
ID
35544
Beschreibung
Comparison Between P2Y12 Antagonist Monotherapy and Dual Antiplatelet Therapy After DES; ODM derived from: https://clinicaltrials.gov/show/NCT02079194
Link
https://clinicaltrials.gov/show/NCT02079194
Stichworte
Versionen (1)
- 08.03.19 08.03.19 -
Rechteinhaber
See clinicaltrials.gov
Hochgeladen am
8. März 2019
DOI
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Lizenz
Creative Commons BY 4.0
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Eligibility Coronary Artery Disease NCT02079194
Eligibility Coronary Artery Disease NCT02079194
- StudyEvent: Eligibility
Ähnliche Modelle
Eligibility Coronary Artery Disease NCT02079194
- StudyEvent: Eligibility
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Age
Item
subject must be at least 20 years of age.
boolean
C0001779 (UMLS CUI [1])
Comprehension Study Protocol | Informed Consent | Informed Consent Patient Representative
Item
subject is able to verbally confirm understandings of risks, benefits and treatment alternatives and he/she or his/her legally authorized representative provides written informed consent prior to any study related procedure.
boolean
C0162340 (UMLS CUI [1,1])
C2348563 (UMLS CUI [1,2])
C0021430 (UMLS CUI [2])
C0021430 (UMLS CUI [3,1])
C0030701 (UMLS CUI [3,2])
C2348563 (UMLS CUI [1,2])
C0021430 (UMLS CUI [2])
C0021430 (UMLS CUI [3,1])
C0030701 (UMLS CUI [3,2])
Percutaneous Coronary Intervention Successful
Item
patients undergoing successful pci
boolean
C1532338 (UMLS CUI [1,1])
C1272703 (UMLS CUI [1,2])
C1272703 (UMLS CUI [1,2])
Hemodynamic instability | Shock, Cardiogenic
Item
hemodynamic instability or cardiogenic shock
boolean
C0948268 (UMLS CUI [1])
C0036980 (UMLS CUI [2])
C0036980 (UMLS CUI [2])
Hemorrhage
Item
active bleeding
boolean
C0019080 (UMLS CUI [1])
Hypersensitivity Investigational New Drugs | Medical contraindication Investigational New Drugs
Item
known hypersensitivity or contraindication to study medications
boolean
C0020517 (UMLS CUI [1,1])
C0013230 (UMLS CUI [1,2])
C1301624 (UMLS CUI [2,1])
C0013230 (UMLS CUI [2,2])
C0013230 (UMLS CUI [1,2])
C1301624 (UMLS CUI [2,1])
C0013230 (UMLS CUI [2,2])
Childbearing Potential | Planned Pregnancy Possible | Exception Pregnancy test negative
Item
female of childbearing potential, unless a recent pregnancy test is negative, who possibly plan to become pregnant any time after enrollment into this study
boolean
C3831118 (UMLS CUI [1])
C0032992 (UMLS CUI [2,1])
C0332149 (UMLS CUI [2,2])
C1705847 (UMLS CUI [3,1])
C0427780 (UMLS CUI [3,2])
C0032992 (UMLS CUI [2,1])
C0332149 (UMLS CUI [2,2])
C1705847 (UMLS CUI [3,1])
C0427780 (UMLS CUI [3,2])
Comorbidity | Exception Heart Diseases | Life Expectancy | Compliance behavior Lacking
Item
non-cardiac co-morbid conditions are present with life expectancy <2 year or that may result in protocol non-compliance (per site investigator's medical judgment).
boolean
C0009488 (UMLS CUI [1])
C1705847 (UMLS CUI [2,1])
C0018799 (UMLS CUI [2,2])
C0023671 (UMLS CUI [3])
C1321605 (UMLS CUI [4,1])
C0332268 (UMLS CUI [4,2])
C1705847 (UMLS CUI [2,1])
C0018799 (UMLS CUI [2,2])
C0023671 (UMLS CUI [3])
C1321605 (UMLS CUI [4,1])
C0332268 (UMLS CUI [4,2])
Exclusion Criteria Angiography
Item
angiographic exclusion criteria
boolean
C0680251 (UMLS CUI [1,1])
C0002978 (UMLS CUI [1,2])
C0002978 (UMLS CUI [1,2])
Bifurcation lesion | Requirement Side Branch Stenting
Item
bifurcation lesions requiring side branch stenting
boolean
C1299363 (UMLS CUI [1])
C1514873 (UMLS CUI [2,1])
C0441987 (UMLS CUI [2,2])
C0500459 (UMLS CUI [2,3])
C2348535 (UMLS CUI [2,4])
C1514873 (UMLS CUI [2,1])
C0441987 (UMLS CUI [2,2])
C0500459 (UMLS CUI [2,3])
C2348535 (UMLS CUI [2,4])
Lesions | Stent overlapped Quantity
Item
lesions treated with 3 or more overlapped stents
boolean
C0221198 (UMLS CUI [1])
C0038257 (UMLS CUI [2,1])
C0185027 (UMLS CUI [2,2])
C1265611 (UMLS CUI [2,3])
C0038257 (UMLS CUI [2,1])
C0185027 (UMLS CUI [2,2])
C1265611 (UMLS CUI [2,3])