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The primary study endpoints were technical success and safety.
Because this is a first-in-humans application of human MSCs in patients with moderate-severe ARDS, the primary study endpoints for both phase 1 and phase 2 will focus on the safety and tolerability of the human MSCs product.
However, the primary study endpoints did not improve significantly.
The primary study endpoints were vein occlusion and absence of reflux, as determined by DUS.
Primary study endpoints were pressure values and the number and volume of air bubbles.
The primary study endpoints of the present contribution were as follows.
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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.
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