ID

12466

Descrizione

The timing of intervention study is a prospective, randomized, international, multicentre comparison of the relative efficacy, safety, and cost effectiveness of a management strategy of coronary angiography and intervention performed within 24 hours of randomization versus delayed coronary angiography and intervention in patients after 36 hours with acute coronary syndromes (ACS). https://clinicaltrials.gov/ct2/show/NCT00552513

collegamento

https://clinicaltrials.gov/ct2/show/NCT00552513

Keywords

versioni (2)
  1. 28/07/15 28/07/15 -
  2. 21/11/15 21/11/15 -
Caricato su

21 novembre 2015

DOI

Per favore, per richiedere un accesso.

Licenza

Creative Commons BY 4.0
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Eligibility TIMACS Acute Coronary Syndrome NCT00552513

Inglese

Eligibility Criteria

1 moduli  
  1. StudyEvent: ODM
    1. Eligibility Criteria
Inclusion Criteria
Descrizione

Inclusion Criteria

Patients presenting or admitted to hospital with symptoms suspected to represent an acute coronary syndrome (unstable angina or MI without persistent ST elevation)
Descrizione

Patients presenting or admitted to hospital with symptoms suspected to represent an acute coronary syndrome (unstable angina or MI without persistent ST elevation)

Tipo di dati

boolean

Alias
UMLS CUI-1
C0948089
Able to randomise within 24 hours of the onset of the most recent episode of symptoms
Descrizione

Able to randomise within 24 hours of the onset of the most recent episode of symptoms

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0034656
Age more than or equal to 60 years
Descrizione

Age more than or equal to 60 years

Tipo di dati

boolean

Alias
UMLS CUI-1
C0001779
Troponin T above the upper limit of normal for the local institution
Descrizione

Troponin T above the upper limit of normal for the local institution

Tipo di dati

boolean

Alias
UMLS CUI-1
C1141947
Troponin I above the upper limit of normal for the local institution
Descrizione

Troponin I above the upper limit of normal for the local institution

Tipo di dati

boolean

Alias
UMLS CUI-1
C0920210
Creatine Kinase - Myocardial Bands (CK-MB) above the upper limit of normal for the local institution
Descrizione

Creatine Kinase - Myocardial Bands (CK-MB) above the upper limit of normal for the local institution

Tipo di dati

boolean

Alias
UMLS CUI-1
C0523584
Written informed consent dated and signed
Descrizione

Written informed consent dated and signed

Tipo di dati

boolean

Alias
UMLS CUI-1
C0021430
Exclusion Criteria
Descrizione

Exclusion Criteria

Age less than 21 years
Descrizione

Age less than 21 years

Tipo di dati

boolean

Alias
UMLS CUI-1
C0001779
Not a suitable candidate for revascularisation
Descrizione

Not a suitable candidate for revascularisation

Tipo di dati

boolean

Alias
UMLS CUI-1
C0027056
Co-morbid condition with life expectancy less than six months
Descrizione

Co-morbid condition with life expectancy less than six months

Tipo di dati

boolean

Alias
UMLS CUI-1
C0679247
Ritorna all'inizio della pagina

Similar models

Eligibility Criteria

1 moduli
  1. StudyEvent: ODM
    1. Eligibility Criteria
Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
Alias
Item Group
Inclusion Criteria
Acute coronary syndrome
Item
Patients presenting or admitted to hospital with symptoms suspected to represent an acute coronary syndrome (unstable angina or MI without persistent ST elevation)
boolean
C0948089 (UMLS CUI-1)
Randomization
Item
Able to randomise within 24 hours of the onset of the most recent episode of symptoms
boolean
C0034656 (UMLS CUI [1])
Age
Item
Age more than or equal to 60 years
boolean
C0001779 (UMLS CUI-1)
Troponin T
Item
Troponin T above the upper limit of normal for the local institution
boolean
C1141947 (UMLS CUI-1)
Troponin I
Item
Troponin I above the upper limit of normal for the local institution
boolean
C0920210 (UMLS CUI-1)
CK-MB
Item
Creatine Kinase - Myocardial Bands (CK-MB) above the upper limit of normal for the local institution
boolean
C0523584 (UMLS CUI-1)
Informed consent
Item
Written informed consent dated and signed
boolean
C0021430 (UMLS CUI-1)
Item Group
Exclusion Criteria
Age
Item
Age less than 21 years
boolean
C0001779 (UMLS CUI-1)
Myocardial Revascularization
Item
Not a suitable candidate for revascularisation
boolean
C0027056 (UMLS CUI-1)
Terminal illness
Item
Co-morbid condition with life expectancy less than six months
boolean
C0679247 (UMLS CUI-1)
Ritorna all'inizio della pagina 

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