Status | Study |
Not yet recruiting |
Study Name: In-hospital and Long-term Outcomes for Percutaneous Chronic Total Coronary Occlusion Revascularization in a High-volume, Multi-operator Program Condition: Ischemic Heart Disease Date: 2013-09-12 |
Active, not recruiting |
Study Name: A Randomized Multicentre Trial to Evaluate the Utilization of Revascularization or Optimal Medical Therapy for the Treatment of Chronic Total Coronary Occlusions Condition: Chronic Stable Angina Dyspnea Corona Date: 2013-01-01 Interventions: Device: Biolimus-eluting stent implantation Recanalization of chronic coronary artery occlusion and subs |
Active, not recruiting |
Study Name: Hybrid Sirolimus-eluting Versus Everolimus-eluting Stents for Total Coronary Occlusions Condition: Coronary Artery Disease Coronary Disease Coronary Stenosis Date: 2011-11-15 Interventions: Device: Hybrid sirolimus- and everolimus-eluting stents (ORSIRO, XIENCE PRIME) Recanalization of totally |
Completed |
Study Name: Systematic Screening for Risk-factors for Ulcer Bleeding Before Anti-thrombotic Treatment Condition: Coronary Occlusion/Thrombosis Peptic Ulcer Hemorrhage Date: 2011-09-26 Interventions: Other: Screening for risk factors for ulcer bleeding Follo |
Completed |
Study Name: Effects of N-acetylcysteine on Pulmonary Function in High-risk Patients Undergoing Off-pump Coronary Bypass Surgery Condition: Coronary Artery Occlusion Date: 2009-11-25 Interventions: Drug: N-acetylcysteine, saline Inject 100 mg/kg of N-acetylcysteine or the equivalent amount of saline f |
Completed |
Study Name: AngiographiC Evaluation of the Everolimus-Eluting Stent in Chronic Total Occlusions - the ACE-CTO Study Condition: Coronary Occlusions Date: 2009-11-12 Interventions: Device: everolimus-eluting stent everolimus-eluting stent (Xience, Abbott Vascular) or Promus (Boston Sc |
Completed |
Study Name: Guidewire for Chronic Total Occlusion Condition: Coronary Occlusion Date: 2009-09-29 Interventions: Device: Percutaneous coronary intervention (PCI) PCI for chronic total occlusion is performed using eith |
Completed |
Study Name: Non-acute Coronary occlusIon Treated By Everolimus ELuting Stent Condition: Coronary Artery Disease Coronary Occlusion Date: 2008-11-17 Interventions: Device: Implantation of sirolimus-eluting coronary stent |
Active, not recruiting |
Study Name: AngelMed for Early Recognition and Treatment of STEMI Condition: Acute Myocardial Infarction (AMI) Coronary Occlusion Date: 2008-10-24 Interventions: Device: Guardian System There is no intervention in this study. The device is a diagnostic only. |
Completed |
Study Name: Safety and Efficacy of the CiTop™ Guidewire for Crossing Chronic Total Occlusions in Coronary Arteries Condition: Coronary Occlusion Date: 2008-01-28 Interventions: Device: CiTop(tm) Guidewire CiTop(tm)6 Guidewire |