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MedAlliance announces completion of enrollment in Japanese SELUTION SLR Study
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MedAlliance announces completion of enrollment in Japanese SELUTION SLR™ Study
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NYON, Switzerland, Jan. 28, 2021 /PRNewswire/ 12-month results from the PRESTIGE Below-the-Knee (BTK) study have been presented as a Late Breaking Trial at LINC 2021. The objective of this clinical investigation has been to evaluate safety and performance outcomes of SELUTION SLR™, MedAlliance s novel sirolimus-eluting balloon, for the treatment of long tibial occlusive lesions (TASC C & D) in patients with Critical Limb Ischemia (CLI).
12-Month Below-the-Knee Data with MedAlliance s SELUTION SLR™ Presented as Late Breaking Trial at LINC
The Primary Patency Rate was 78% and the rate of wound healing was 81%. Freedom from Target Lesion Revascularization (TLR) was exhibited by 93% of patients and 84% demonstrated Amputation Free Survival (AFS). All these figures have been sustained from the six-month data.
12-Month Below-the-Knee Data with MedAlliance s SELUTION SLR Presented as Late Breaking Trial at LINC
NYON, Switzerland, Jan. 28, 2021 /PRNewswire/ 12-month results from the PRESTIGE Below-the-Knee (BTK) study have been presented as a Late Breaking Trial at LINC 2021. The objective of this clinical investigation has been to evaluate safety and performance outcomes of SELUTION SLR, MedAlliance s novel sirolimus-eluting balloon, for the treatment of long tibial occlusive lesions (TASC C & D) in patients with Critical Limb Ischemia (CLI).
The Primary Patency Rate was 78% and the rate of wound healing was 81%. Freedom from Target Lesion Revascularization (TLR) was exhibited by 93% of patients and 84% demonstrated Amputation Free Survival (AFS). All these figures have been sustained from the six-month data.
28 gennaio 2021 17:40
Fonte: Adnkronos
#salute-e-benessere
NYON, Switzerland, Jan. 28, 2021 /PRNewswire/ 12-month results from the PRESTIGE Below-the-Knee (BTK) study have been presented as a Late Breaking Trial at LINC 2021. The objective of this clinical investigation has been to evaluate safety and performance outcomes of SELUTION SLR™, MedAlliance s novel sirolimus-eluting balloon, for the treatment of long tibial occlusive lesions (TASC C & D) in patients with Critical Limb Ischemia (CLI).
The Primary Patency Rate was 78% and the rate of wound healing was 81%. Freedom from Target Lesion Revascularization (TLR) was exhibited by 93% of patients and 84% demonstrated Amputation Free Survival (AFS). All these figures have been sustained from the six-month data.
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