Information:
Error:
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
Link
https://clinicaltrials.gov/ct2/show/NCT00089895
Keywords
Versions (1)
- 7/28/15 7/28/15 -
Uploaded on
July 28, 2015
DOI
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License
Creative Commons BY 4.0
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Eligibility EARLY ACS Acute Coronary Syndrome NCT00089895
Similar models
Eligibility criteria
- StudyEvent: ODM
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
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)
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)