ID

34232

Beschreibung

POLish Bifurcation Optimal Stenting Study; ODM derived from: https://clinicaltrials.gov/show/NCT02192840

Link

https://clinicaltrials.gov/show/NCT02192840

Stichworte

  1. 15.01.19 15.01.19 -
Rechteinhaber

see on clinicaltrials.gov

Hochgeladen am

15. Januar 2019

DOI

Für eine Beantragung loggen Sie sich ein.

Lizenz

Creative Commons BY 4.0

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 :

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

Eligibility Coronary Artery Disease NCT02192840

Eligibility Coronary Artery Disease NCT02192840

Inclusion Criteria
Beschreibung

Inclusion Criteria

Alias
UMLS CUI
C1512693
subject able to verbally confirm understandings of risks, benefits of receiving pci for true bifurcation lesions, and he/she or his/her legally authorized representative provides written informed consent prior to any study related procedure.
Beschreibung

ID.1

Datentyp

boolean

target main branch lesion(s) located in a native coronary artery with diameter of ≥
Beschreibung

ID.2

Datentyp

boolean

2.5 mm and ≤ 4.5 mm. target side branch lesion(s) located in a native coronary artery with diameter of ≥ 2.0 mm.
Beschreibung

ID.3

Datentyp

boolean

target lesion(s) amenable for pci with balloon angioplasty of the side branch.
Beschreibung

ID.4

Datentyp

boolean

Exclusion Criteria
Beschreibung

Exclusion Criteria

Alias
UMLS CUI
C0680251
stemi
Beschreibung

ID.5

Datentyp

boolean

non-cardiac co-morbid conditions are present with life expectancy <1 year or that may result in protocol non-compliance (per site investigator's medical judgment).
Beschreibung

ID.6

Datentyp

boolean

subjects who refuse to give informed consent.
Beschreibung

ID.7

Datentyp

boolean

subjects with lvef<30%
Beschreibung

ID.8

Datentyp

boolean

subjects with moderate or severe degree valvular heart disease or primary cardiomyopathy
Beschreibung

ID.9

Datentyp

boolean

Ähnliche Modelle

Eligibility Coronary Artery Disease NCT02192840

Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
subject able to verbally confirm understandings of risks, benefits of receiving pci for true bifurcation lesions, and he/she or his/her legally authorized representative provides written informed consent prior to any study related procedure.
boolean
ID.2
Item
target main branch lesion(s) located in a native coronary artery with diameter of ≥
boolean
ID.3
Item
2.5 mm and ≤ 4.5 mm. target side branch lesion(s) located in a native coronary artery with diameter of ≥ 2.0 mm.
boolean
ID.4
Item
target lesion(s) amenable for pci with balloon angioplasty of the side branch.
boolean
Item Group
C0680251 (UMLS CUI)
ID.5
Item
stemi
boolean
ID.6
Item
non-cardiac co-morbid conditions are present with life expectancy <1 year or that may result in protocol non-compliance (per site investigator's medical judgment).
boolean
ID.7
Item
subjects who refuse to give informed consent.
boolean
ID.8
Item
subjects with lvef<30%
boolean
ID.9
Item
subjects with moderate or severe degree valvular heart disease or primary cardiomyopathy
boolean

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