Status:
TERMINATED
The Effect Of Acadesine On Reducing Cardiovascular and Cerebrovascular Adverse Events In Coronary Artery Bypass Graft (CABG) Surgery (Study P05633 AM1)(TERMINATED)
Lead Sponsor:
Merck Sharp & Dohme LLC
Collaborating Sponsors:
Duke Clinical Research Institute
Conditions:
Coronary Artery Bypass
Myocardial Infarction
Eligibility:
All Genders
50+ years
Phase:
PHASE3
Brief Summary
The purpose of this study is to determine whether acadesine is effective in reducing the cardiovascular and cerebrovascular adverse events in high-risk participants undergoing CABG surgery.
Eligibility Criteria
Inclusion
- A high risk participant undergoing non emergency CABG surgery requiring CPB and cardioplegia.
- Age: \>=50 years
- At least one of the following risk factors:
- Female (but not pregnant or lactating), or
- History of prior CABG, or
- History of myocardial infarction (MI), or
- History of ischemic stroke, or
- Left ventricular ejection fraction \<=30%, or
- Diabetes mellitus requiring insulin and/or antidiabetic agents.
- Significant coronary artery stenosis
Exclusion
- Planned valve replacement, carotid artery or aortic surgery, distal coronary endarterectomy,surgical ablation for cardiac arrhythmia, or ventricular aneurysmectomy, alone or with CABG surgery (repair for mild to moderate mitral valve disease with concomitant CABG is not excluded).
- Planned or staged major surgery within 30 days of CABG surgery
- CABG surgery using intermittent aortic cross clamping without cardioplegia.
- Minimally invasive surgery (ie, without use of CPB).
- MI within 5 days prior to surgery.
- Pre-operative or planned intra operative/postoperative use of intra-aortic balloon pump (IABP), ventricular assist device (VAD), extra-corporeal membrane oxygenator (ECMO), or other mechanical hemodynamic assist device.
- History or presence of gout or uric acid nephrolithiasis.
- Serum creatinine \>2 mg/dL (180 µmol/L).
- Serum alanine aminotransferase (ALT) or aspartate aminotransferase (AST) \>2 x Upper Limit of Normal (ULN).
- Adenosine, aminophylline, nicotinic acid, pentoxifylline, theophylline, and any cardioplegia solution containing adenosine, dipyridamole or lidoflazine within 24 hours before surgery:
- Dipyridamole within 2 days and allopurinol or febuxostat within 4 days before surgery
- Food and drinks containing caffeine, theobromines or methylxanthines (such as coffee, tea, colas, some 'energy' drinks or chocolate) within 12 hours before surgery.
- Pregnancy
Key Trial Info
Start Date :
April 1 2009
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
October 1 2010
Estimated Enrollment :
3080 Patients enrolled
Trial Details
Trial ID
NCT00872001
Start Date
April 1 2009
End Date
October 1 2010
Last Update
October 29 2015
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