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The primary study endpoint is graft patency as determined by angiography, 8 12 months postoperatively.
The primary study endpoint is a composite of cardiovascular mortality and morbidity.
The primary study endpoint is VO2peak.
The primary study endpoint was 90-daysmortality.
The primary study endpoint is VO₂peak, as measured by an incremental cardiopulmonary exercise test.
The main primary study endpoint was percent correction of the serum potassium after 24 h.
The primary study endpoint was the percentage change in target fibroid perfused volume as assessed by contrast-enhanced MRI at baseline and again at 3 months.
The primary study endpoint was the percentage change in perfused fibroid volume, as assessed by contrast-enhanced MRI at 3 months.
A core MRI facility was used to reduce variability and bias in MRI imaging quality, interpretation, and measurements relative to the primary study endpoint.
The primary study endpoint success criterion was achievement of >30 % reduction in mean target fibroid perfused volume in at least 50%% of patients.
The primary study endpoint was the first occurrence of CHD death or nonfatal myocardial infarction.
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