ID

20447

Beschreibung

Systemic Treatment With Everolimus for the Prevention of MACE After Bare Metal Stent Implantation; ODM derived from: https://clinicaltrials.gov/show/NCT00426049

Link

https://clinicaltrials.gov/show/NCT00426049

Stichworte

Versionen (1)
  1. 22.02.17 22.02.17 -
Hochgeladen am

22. Februar 2017

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.

Zurück zu Modell Kommentaren
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 NCT00426049

Englisch

Eligibility Coronary Artery Disease NCT00426049

1 Formulare  
Inclusion Criteria
Beschreibung

Inclusion Criteria

Alias
UMLS CUI
C1512693
1. males or females, aged >18 years.
Beschreibung

Age

Datentyp

boolean

Alias
UMLS CUI [1]
C0001779
2. patients with coronary artery disease who are scheduled for coronary intervention with bare metal stent placement for treatment of de novo or first restenosis in a native coronary artery.
Beschreibung

Coronary Artery Disease | Intervention Coronary Scheduled | Bare metal coronary stent placement | Coronary Restenosis de novo | Coronary Restenosis First

Datentyp

boolean

Alias
UMLS CUI [1]
C1956346
UMLS CUI [2,1]
C0184661
UMLS CUI [2,2]
C1522318
UMLS CUI [2,3]
C0205539
UMLS CUI [3]
C2609297
UMLS CUI [4,1]
C0948480
UMLS CUI [4,2]
C1515568
UMLS CUI [5,1]
C0948480
UMLS CUI [5,2]
C0205435
3. target lesion must be in a native coronary vessel of 2.25 – 4.0 mm size.
Beschreibung

Target Lesion Coronary Vessel size

Datentyp

boolean

Alias
UMLS CUI [1,1]
C2986546
UMLS CUI [1,2]
C0010075
UMLS CUI [1,3]
C0456389
4. target lesion has to be of less than or equal to 25 mm length.
Beschreibung

Target Lesion Length

Datentyp

boolean

Alias
UMLS CUI [1,1]
C2986546
UMLS CUI [1,2]
C1444754
5. tandem lesion may be included as long as:
Beschreibung

Lesion Double

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0221198
UMLS CUI [1,2]
C0205173
overall length is less than or equal to 25 mm
Beschreibung

Lesion Double Length

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0221198
UMLS CUI [1,2]
C0205173
UMLS CUI [1,3]
C1444754
tandem lesion will be treated with one stent and counted as one lesion.
Beschreibung

Lesion Double Therapeutic procedure Stent Single

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0221198
UMLS CUI [1,2]
C0205173
UMLS CUI [1,3]
C0087111
UMLS CUI [1,4]
C0038257
UMLS CUI [1,5]
C0205171
Exclusion Criteria
Beschreibung

Exclusion Criteria

Alias
UMLS CUI
C0680251
the following exclusion criteria must not be present at baseline visit 1 (bl1, screening visit prior to coronary intervention). if an exclusion criterion occurred afterwards, e.g., during the coronary intervention, the patient must be excluded from the study.
Beschreibung

Exclusion Criteria Occurrence Timepoint

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0680251
UMLS CUI [1,2]
C2745955
UMLS CUI [1,3]
C2348792
1. target lesion has a reference vessel size of less than 2.25 or more than 4.0 mm diameter.
Beschreibung

Target Lesion Reference Vessel size

Datentyp

boolean

Alias
UMLS CUI [1,1]
C2986546
UMLS CUI [1,2]
C0005847
UMLS CUI [1,3]
C1706462
UMLS CUI [1,4]
C0456389
2. target lesion is a total occlusion or located at a bifurcation.
Beschreibung

Target Lesion Obstruction Total | Target Lesion Location Coronary Vessel Bifurcation

Datentyp

boolean

Alias
UMLS CUI [1,1]
C2986546
UMLS CUI [1,2]
C0028778
UMLS CUI [1,3]
C0439810
UMLS CUI [2,1]
C2986546
UMLS CUI [2,2]
C0450429
UMLS CUI [2,3]
C3640041
3. treatment affords implantation of more than one stent per treated lesion.
Beschreibung

Lesion Therapeutic procedure Stent Quantity

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0221198
UMLS CUI [1,2]
C0087111
UMLS CUI [1,3]
C0038257
UMLS CUI [1,4]
C1265611
4. target lesion was already treated by brachytherapy.
Beschreibung

Brachytherapy Target Lesion

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0006098
UMLS CUI [1,2]
C2986546
5. target lesion has one or more of the following criteria:
Beschreibung

Target Lesion criteria

Datentyp

boolean

Alias
UMLS CUI [1,1]
C2986546
UMLS CUI [1,2]
C0243161
left main lesion
Beschreibung

Left coronary artery main stem Lesion

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0226031
UMLS CUI [1,2]
C0221198
ostial lesion of the rca
Beschreibung

Ostium of right coronary artery Lesion

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0226045
UMLS CUI [1,2]
C0221198
located at less than 2 mm after the origin of the lad or rcx.
Beschreibung

Target Lesion Location Anterior descending branch of left coronary artery | Target Lesion Location circumflex branch of left coronary artery

Datentyp

boolean

Alias
UMLS CUI [1,1]
C2986546
UMLS CUI [1,2]
C0450429
UMLS CUI [1,3]
C0226032
UMLS CUI [2,1]
C2986546
UMLS CUI [2,2]
C0450429
UMLS CUI [2,3]
C0226037
other protocol defined inclusion/exclusion criteria may apply.
Beschreibung

Clinical Trial Eligibility Criteria Study Protocol

Datentyp

boolean

Alias
UMLS CUI [1,1]
C1516637
UMLS CUI [1,2]
C2348563
Zum Seitenanfang zurückkehren

Ähnliche Modelle

Eligibility Coronary Artery Disease NCT00426049

1 Formulare
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
C1512693 (UMLS CUI)
Age
Item
1. males or females, aged >18 years.
boolean
C0001779 (UMLS CUI [1])
Coronary Artery Disease | Intervention Coronary Scheduled | Bare metal coronary stent placement | Coronary Restenosis de novo | Coronary Restenosis First
Item
2. patients with coronary artery disease who are scheduled for coronary intervention with bare metal stent placement for treatment of de novo or first restenosis in a native coronary artery.
boolean
C1956346 (UMLS CUI [1])
C0184661 (UMLS CUI [2,1])
C1522318 (UMLS CUI [2,2])
C0205539 (UMLS CUI [2,3])
C2609297 (UMLS CUI [3])
C0948480 (UMLS CUI [4,1])
C1515568 (UMLS CUI [4,2])
C0948480 (UMLS CUI [5,1])
C0205435 (UMLS CUI [5,2])
Target Lesion Coronary Vessel size
Item
3. target lesion must be in a native coronary vessel of 2.25 – 4.0 mm size.
boolean
C2986546 (UMLS CUI [1,1])
C0010075 (UMLS CUI [1,2])
C0456389 (UMLS CUI [1,3])
Target Lesion Length
Item
4. target lesion has to be of less than or equal to 25 mm length.
boolean
C2986546 (UMLS CUI [1,1])
C1444754 (UMLS CUI [1,2])
Lesion Double
Item
5. tandem lesion may be included as long as:
boolean
C0221198 (UMLS CUI [1,1])
C0205173 (UMLS CUI [1,2])
Lesion Double Length
Item
overall length is less than or equal to 25 mm
boolean
C0221198 (UMLS CUI [1,1])
C0205173 (UMLS CUI [1,2])
C1444754 (UMLS CUI [1,3])
Lesion Double Therapeutic procedure Stent Single
Item
tandem lesion will be treated with one stent and counted as one lesion.
boolean
C0221198 (UMLS CUI [1,1])
C0205173 (UMLS CUI [1,2])
C0087111 (UMLS CUI [1,3])
C0038257 (UMLS CUI [1,4])
C0205171 (UMLS CUI [1,5])
Item Group
C0680251 (UMLS CUI)
Exclusion Criteria Occurrence Timepoint
Item
the following exclusion criteria must not be present at baseline visit 1 (bl1, screening visit prior to coronary intervention). if an exclusion criterion occurred afterwards, e.g., during the coronary intervention, the patient must be excluded from the study.
boolean
C0680251 (UMLS CUI [1,1])
C2745955 (UMLS CUI [1,2])
C2348792 (UMLS CUI [1,3])
Target Lesion Reference Vessel size
Item
1. target lesion has a reference vessel size of less than 2.25 or more than 4.0 mm diameter.
boolean
C2986546 (UMLS CUI [1,1])
C0005847 (UMLS CUI [1,2])
C1706462 (UMLS CUI [1,3])
C0456389 (UMLS CUI [1,4])
Target Lesion Obstruction Total | Target Lesion Location Coronary Vessel Bifurcation
Item
2. target lesion is a total occlusion or located at a bifurcation.
boolean
C2986546 (UMLS CUI [1,1])
C0028778 (UMLS CUI [1,2])
C0439810 (UMLS CUI [1,3])
C2986546 (UMLS CUI [2,1])
C0450429 (UMLS CUI [2,2])
C3640041 (UMLS CUI [2,3])
Lesion Therapeutic procedure Stent Quantity
Item
3. treatment affords implantation of more than one stent per treated lesion.
boolean
C0221198 (UMLS CUI [1,1])
C0087111 (UMLS CUI [1,2])
C0038257 (UMLS CUI [1,3])
C1265611 (UMLS CUI [1,4])
Brachytherapy Target Lesion
Item
4. target lesion was already treated by brachytherapy.
boolean
C0006098 (UMLS CUI [1,1])
C2986546 (UMLS CUI [1,2])
Target Lesion criteria
Item
5. target lesion has one or more of the following criteria:
boolean
C2986546 (UMLS CUI [1,1])
C0243161 (UMLS CUI [1,2])
Left coronary artery main stem Lesion
Item
left main lesion
boolean
C0226031 (UMLS CUI [1,1])
C0221198 (UMLS CUI [1,2])
Ostium of right coronary artery Lesion
Item
ostial lesion of the rca
boolean
C0226045 (UMLS CUI [1,1])
C0221198 (UMLS CUI [1,2])
Target Lesion Location Anterior descending branch of left coronary artery | Target Lesion Location circumflex branch of left coronary artery
Item
located at less than 2 mm after the origin of the lad or rcx.
boolean
C2986546 (UMLS CUI [1,1])
C0450429 (UMLS CUI [1,2])
C0226032 (UMLS CUI [1,3])
C2986546 (UMLS CUI [2,1])
C0450429 (UMLS CUI [2,2])
C0226037 (UMLS CUI [2,3])
Clinical Trial Eligibility Criteria Study Protocol
Item
other protocol defined inclusion/exclusion criteria may apply.
boolean
C1516637 (UMLS CUI [1,1])
C2348563 (UMLS CUI [1,2])
Zum Seitenanfang zurückkehren 

Kontakt

Benutzen Sie dieses Formular für Rückmeldungen, Fragen und Verbesserungsvorschläge.

Mit * gekennzeichnete Felder sind notwendig.

Hilfe

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