ID

11717

Beskrivning

The purpose of this study is to test the hypothesis that the inhibition of the renin-angiotensin-aldosterone system (RAAS) with the angiotensin receptor blocker valsartan or the renin antagonist aliskiren will improve ventricular hemodynamics, as reflected by a greater reduction in levels of N-terminal proB-type natriuretic peptide (NT-proBNP) compared to placebo in subjects stabilized following acute coronary syndrome (ACS) who are determined to be at high risk due to an elevated concentration of natriuretic peptides. https://clinicaltrials.gov/ct2/show/NCT00409578

Länk

https://clinicaltrials.gov/ct2/show/NCT00409578

Nyckelord

  1. 2015-07-28 2015-07-28 -
Uppladdad den

28 juli 2015

DOI

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Licens

Creative Commons BY 4.0

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Eligibility Aliskiren and Valsartan Acute Coronary Syndrome NCT00409578

Eligibility Criteria

  1. StudyEvent: ODM
    1. Eligibility Criteria
Inclusion Criteria
Beskrivning

Inclusion Criteria

Male or female outpatients
Beskrivning

Male or female outpatients

Datatyp

boolean

Alias
UMLS CUI-1
C0079399
18 years old or older
Beskrivning

18 years old or older

Datatyp

boolean

Alias
UMLS CUI-1
C0001779
Final diagnosis of acute coronary syndrome
Beskrivning

Final diagnosis of acute coronary syndrome

Datatyp

boolean

Alias
UMLS CUI-1
C0948089
ischemic chest discomfort
Beskrivning

ischemic chest discomfort

Datatyp

boolean

Alias
UMLS CUI-1
C0008031
Elevated concentrations of natriuretic peptide 3-10 days after admission for their qualifying acute coronary syndrome event
Beskrivning

Elevated concentrations of natriuretic peptide 3-10 days after admission for their qualifying acute coronary syndrome event

Datatyp

boolean

Alias
UMLS CUI-1
C1095989
Exclusion criteria
Beskrivning

Exclusion criteria

Presence of clinically overt heart failure
Beskrivning

Presence of clinically overt heart failure

Datatyp

boolean

Alias
UMLS CUI-1
C0018801
Known evidence of left ventricular systolic dysfunction
Beskrivning

Known evidence of left ventricular systolic dysfunction

Datatyp

boolean

Alias
UMLS CUI-1
C1277187
Percutaneous coronary intervention (PCI) less than 24 hours before randomization
Beskrivning

Percutaneous coronary intervention (PCI) less than 24 hours before randomization

Datatyp

boolean

Alias
UMLS CUI-1
C1532338
chronic ACEI therapy
Beskrivning

chronic ACEI therapy

Datatyp

boolean

Alias
UMLS CUI-1
C0003015
chronic ARB therapy
Beskrivning

chronic ARB therapy

Datatyp

boolean

Alias
UMLS CUI-1
C0521942

Similar models

Eligibility Criteria

  1. StudyEvent: ODM
    1. Eligibility Criteria
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
Inclusion Criteria
Gender
Item
Male or female outpatients
boolean
C0079399 (UMLS CUI-1)
Age
Item
18 years old or older
boolean
C0001779 (UMLS CUI-1)
Acute coronary syndrome
Item
Final diagnosis of acute coronary syndrome
boolean
C0948089 (UMLS CUI-1)
Chest pain
Item
ischemic chest discomfort
boolean
C0008031 (UMLS CUI-1)
BNP
Item
Elevated concentrations of natriuretic peptide 3-10 days after admission for their qualifying acute coronary syndrome event
boolean
C1095989 (UMLS CUI-1)
Item Group
Exclusion criteria
Heart failure
Item
Presence of clinically overt heart failure
boolean
C0018801 (UMLS CUI-1)
Left ventricular systolic dysfunction
Item
Known evidence of left ventricular systolic dysfunction
boolean
C1277187 (UMLS CUI-1)
PCI
Item
Percutaneous coronary intervention (PCI) less than 24 hours before randomization
boolean
C1532338 (UMLS CUI-1)
ACE inhibitors
Item
chronic ACEI therapy
boolean
C0003015 (UMLS CUI-1)
ARB
Item
chronic ARB therapy
boolean
C0521942 (UMLS CUI-1)

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