ID

11712

Description

The purpose of this study is to see if early INTEGRILIN® (eptifibatide) therapy in patients with non-ST-segment elevation acute coronary syndrome (ACS) reduces the occurence of death, heart attack and urgent cardiac intervention (surgery) compared to placebo (with delayed provisional use of eptifibatide). https://clinicaltrials.gov/ct2/show/NCT00089895

Lien

https://clinicaltrials.gov/ct2/show/NCT00089895

Mots-clés

Versions (1)
  1. 28/07/2015 28/07/2015 -
Téléchargé le

28 juillet 2015

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0
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Eligibility EARLY ACS Acute Coronary Syndrome NCT00089895

Anglais

Eligibility criteria

1 Formulaires  
  1. StudyEvent: ODM
    1. Eligibility criteria
Inclusion Criteria
Description

Inclusion Criteria

Willing and able to give informed consent and comply with study procedures and follow-up through 1 year.
Description

Willing and able to give informed consent and comply with study procedures and follow-up through 1 year.

Type de données

boolean

Alias
UMLS CUI-1
C0021430
symptoms of cardiac ischemia
Description

symptoms of cardiac ischemia

Type de données

boolean

Alias
UMLS CUI-1
C0151744
60 years of age or more
Description

60 years of age or more

Type de données

boolean

Alias
UMLS CUI-1
C0001779
Electrocardiogram changes
Description

Electrocardiogram changes

Type de données

boolean

Alias
UMLS CUI-1
C0855329
Elevated troponin levels
Description

Elevated troponin

Type de données

boolean

Alias
UMLS CUI-1
C0523952
Elevated CK-MB levels
Description

Elevated CK-MB levels

Type de données

boolean

Alias
UMLS CUI-1
C0523584
Prior history of cardiovascular disease
Description

Prior history of cardiovascular disease

Type de données

boolean

Alias
UMLS CUI-1
C0455539
Exclusion criteria
Description

Exclusion criteria

pregnancy (known or suspected)
Description

pregnancy (known or suspected)

Type de données

boolean

Alias
UMLS CUI-1
C0549206
renal dialysis within 30 days prior to randomizing in study
Description

renal dialysis within 30 days prior to randomizing in study

Type de données

boolean

Alias
UMLS CUI-1
C0019004
Stroke
Description

Stroke

Type de données

boolean

Alias
UMLS CUI-1
C0038454
central nervous system damage
Description

central nervous system damage

Type de données

boolean

Alias
UMLS CUI-1
C0007682
bleeding disorders
Description

bleeding disorders

Type de données

boolean

Alias
UMLS CUI-1
C3251812
major surgery
Description

major surgery

Type de données

boolean

Alias
UMLS CUI-1
C0679637
major trauma
Description

major trauma

Type de données

boolean

Alias
UMLS CUI-1
C0332677
treatment with heparin
Description

treatment with heparin

Type de données

boolean

Alias
UMLS CUI-1
C2825026
Treatment with eptifibatide
Description

Treatment with eptifibatide

Type de données

boolean

Alias
UMLS CUI-1
C0253563
Retour au début de la page

Similar models

Eligibility criteria

1 Formulaires
  1. StudyEvent: ODM
    1. Eligibility criteria
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
Inclusion Criteria
Informed consent
Item
Willing and able to give informed consent and comply with study procedures and follow-up through 1 year.
boolean
C0021430 (UMLS CUI-1)
Myocardial Ischemia
Item
symptoms of cardiac ischemia
boolean
C0151744 (UMLS CUI-1)
Age
Item
60 years of age or more
boolean
C0001779 (UMLS CUI-1)
Electrocardiogram change
Item
Electrocardiogram changes
boolean
C0855329 (UMLS CUI-1)
Troponin
Item
Elevated troponin levels
boolean
C0523952 (UMLS CUI-1)
CK-MB
Item
Elevated CK-MB levels
boolean
C0523584 (UMLS CUI-1)
History of cardiovascular disease
Item
Prior history of cardiovascular disease
boolean
C0455539 (UMLS CUI-1)
Item Group
Exclusion criteria
Pregnancy
Item
pregnancy (known or suspected)
boolean
C0549206 (UMLS CUI-1)
Hemodialysis
Item
renal dialysis within 30 days prior to randomizing in study
boolean
C0019004 (UMLS CUI-1)
Stroke
Item
Stroke
boolean
C0038454 (UMLS CUI-1)
CNS disorder
Item
central nervous system damage
boolean
C0007682 (UMLS CUI-1)
Bleeding risk
Item
bleeding disorders
boolean
C3251812 (UMLS CUI-1)
major surgery
Item
major surgery
boolean
C0679637 (UMLS CUI-1)
major injury
Item
major trauma
boolean
C0332677 (UMLS CUI-1)
Heparin
Item
treatment with heparin
boolean
C2825026 (UMLS CUI-1)
Eptifibatide
Item
Treatment with eptifibatide
boolean
C0253563 (UMLS CUI-1)
Retour au début de la page 

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