MADIT ASIA Cardiac Resynchronization Trial

Exclusion Criteria

• •Subject with a currently implanted pacemaker, ICD, CRT-P or CRT-D generator or device component
• •Subject with a history of spontaneous sustained VT\>160 bpm or VF
• •Subject with permanent or chronic AF, or cardioversion for AF within the past 3 calendar months before randomization
• •Subject with structural heart disease such as congenital heart disease, valvular heart disease, e.g., rheumatic valvular heart disease, amyloid heart disease, etc.
• •Subject with coronary artery bypass graft surgery or percutaneous coronary intervention within the past 3 calendar months before randomization
• •Subject with enzyme positive myocardial infarction within the past 3 calendar months prior to randomization
• •Subject with angiographic evidence of coronary disease who are candidates for coronary revascularization and are likely to undergo coronary artery bypass graft surgery or percutaneous coronary intervention in the foreseeable future
• •Right bundle branch block or non-specific interventricular conduction delay
• •Subject with second or third degree heart block
• •Subject in New York Heart Association Class IV (symptoms of heart failure at rest)
• •Subject who is pregnant or plans to become pregnant during the course of the trial. Note: Women of childbearing potential must have a negative pregnancy test within 7 days prior to randomization
• •Subject with irreversible brain damage from pre-existing cerebral disease
• •Subject with presence of any disease, other than the subject's cardiac disease, associated with a reduced likelihood of survival for the duration of the trial, e.g., cancer, uremia, liver failure, etc.
• •Subject with chronic renal disease with blood urea nitrogen (BUN) \> 50mg/dl (18 mmol/l) or creatinine \> 2.5mg/dl (221 µmol/l)
• •Subject participating in any other clinical trial
• •Subject unwilling or unable to cooperate with the protocol
• •Subject who lives at such a distance from the clinic that travel for follow-up visits would be unusually difficult
• •Subject who does not anticipate being a resident of the area for the scheduled duration of the trial
• •Subject unwilling to sign the consent for participation
• •Subject whose physician does not allow participation