A Randomised Controlled Trial of Prostar PlusTMfor Haemostasis in Patients After Coronary Angioplasty
Objectives: to clarify the efficacy and safety of Prostar PlusTM, a new percutaneous vascular surgical device (PVS) for vascular haemostasis. Design: prospective randomised controlled trial. Methods: a consecutive series of 60 patients were randomised to either PVS (n =30) or conventional manual com...
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Veröffentlicht in: | European journal of vascular and endovascular surgery 2000-05, Vol.19 (5), p.451-455 |
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Hauptverfasser: | , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Objectives: to clarify the efficacy and safety of Prostar PlusTM, a new percutaneous vascular surgical device (PVS) for vascular haemostasis. Design: prospective randomised controlled trial. Methods: a consecutive series of 60 patients were randomised to either PVS (n =30) or conventional manual compression ( n=30) following coronary angioplasty or stenting with femoral access using an 8-F sheath. Results: PVS significantly shortened the time to haemostasis (10 s.d. 3 vs. 27 s.d. 9 min, p |
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ISSN: | 1078-5884 1532-2165 |
DOI: | 10.1053/ejvs.1999.1071 |