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Coronary Stenosis clinical trials

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NCT ID: NCT02854007 Recruiting - Clinical trials for Coronary Stenosis Treated With Implant of Bioresorbable Devices

Costs, Effectiveness, QALYs, and Efficiency of Bioabsorbable Devices in Daily Clinical Practice

REPARA-QALY
Start date: June 2016
Phase: N/A
Study type: Observational [Patient Registry]

A multicenter, prospective, observational cohort study with clinical, quality of life, and economic evaluation to ascertain the quality-adjusted life years (QALYs) gained by patients with ischemic heart disease revascularized with Absorb in standard clinical practice in Spain. A before-after comparative analysis will be performed, so that each patient will act as his/her own control.

NCT ID: NCT02792075 Recruiting - Clinical trials for Coronary Artery Disease

Prognosis of Coronary Stenosis Based on Intracoronary Imaging; A Multicenter, Prospective Observational Study

IRIS imaging
Start date: July 2016
Phase:
Study type: Observational

The purpose of this study is to evaluate the prognosis of coronary stenosis based on intracoronary Imaging.

NCT ID: NCT02791113 Recruiting - Clinical trials for Coronary Heart Disease

Analysis of Coronary CT Angiography to Identify Patients With Significant Coronary Artery Stenosis

CTAAnalyzer
Start date: March 2014
Phase: N/A
Study type: Observational

The investigators propose to develop a computational framework involving a novel automatic image segmentation algorithm based on CTA images, an artery model reconstruction algorithm for stenosis detection, and quantification of severity of stenosis in terms of area stenosis.

NCT ID: NCT02634086 Recruiting - Clinical trials for Coronary Artery Disease

Long-term Outcome of Triple-vessel Coronary Artery Disease Underwent Three Different Strategies (LOTUS)

LOTUS
Start date: April 2004
Phase: N/A
Study type: Observational

The study is to determine the long-term outcome of patients with coronary triple vessels disease (TVD) in the real world of China, by three different treatment strategies: percutaneous coronary intervention (PCI), Coronary artery bypass graft (CABG) or optimal medication therapy (OMT).

NCT ID: NCT02421016 Recruiting - Coronary Stenosis Clinical Trials

Test Efficacy With Bioresorbable Polymer Coating Versus Bioresorbable Polymer Backbone (ISAR-RESORB)

Start date: May 2015
Phase: N/A
Study type: Interventional

The bioresorbable polymer SYNERGY EES exhibits a favourable vascular healing profile in patients undergoing coronary intervention for de novo lesions. Specifically, the SYNERGY EES is superior to the ABSORB bioresorbable vascular scaffold in terms of antirestenotic efficacy as assessed by angiography at 6-8 months.

NCT ID: NCT02317081 Recruiting - Clinical trials for Native Coronary Artery Stenosis

Axetis Inert Coronary Stent System First In Man Clinical Investigation (AXETIS FIM)

Start date: February 2014
Phase: N/A
Study type: Interventional

Prospective, multicenter, single arm study, to assess the feasibility and safety of the Axetis Inert Stent for treatment of patients with de novo coronary artery stenosis in native vessels.

NCT ID: NCT02315924 Recruiting - Coronary Stenosis Clinical Trials

Combined Coronary and Cerebral Angiography and Intervention for Coronary and Cerebrovascular Atherosclerosis

Start date: March 2013
Phase: N/A
Study type: Interventional

Intracranial atherosclerosis is common vascular lesion in Asian acute stroke patients and intracranial atherosclerosis patients have high rate of coronary artery disease (CAD). Moreover, several studies showed obvious association of CAD and cerebrovascular stenosis, which had been proved to increase the risk of stroke after coronary revascularization including coronary bypass surgery or percutaneous coronary intervention. In addition, the efficacy and safety of combined coronary and cerebral intervention are not fully investigated. Hence, the aim of this study is to evaluate the prevalence and characteristics of coronary and cerebrovascular arteriosclerosis as measured by combined coronary and cerebral angiography, explore the relationship between inflammation, atherosclerosis-related markers and coronary and cerebral atherosclerosis and compare the efficacy and safety of simultaneous or staged coronary and cerebral interventional strategy in Chinese Patients. The coronary angiography and cerebrovascular angiography are performed for all participants. The combined strategy for coronary and cerebrovascular angiography is carried out routinely in the investigators institutions. Simultaneous strategy is considered as that performed via the same access and within the same day. Staged strategy is intended as that performed within 7 days from the first procedure. The sequence of angiographies is established on an individual patient basis by the cardiovascular and neurointerventional team according to clinical symptoms of the patients and after coronary or cerebrovascular angiography. After combined coronary and cerebral angiography, simultaneous or staged interventional strategy will be performed in patients with severe coronary and cerebral stenosis. Blood sample is obtained from artery sheath when performing coronary or cerebral angiography. Lipid levels, inflammation and atherosclerosis-related markers will be measured in this study.

NCT ID: NCT01971749 Recruiting - Clinical trials for Unprotected Left Main Coronary Artery Stenosis

Register of Treatment of Unprotected Left Main Coronary Artery Stenosis in Andalucía

RETRATO
Start date: May 2013
Phase: N/A
Study type: Observational [Patient Registry]

Register of treatment of unprotected left main coronary artery stenosis in Andalucia (RETRATO).

NCT ID: NCT01915420 Recruiting - Clinical trials for Coronary Artery Disease

The ASSURE ROT Registry: Bioresorbable Vascular Scaffold Following Rotablation for Complex Coronary Lesions

ASSURE ROT
Start date: August 2013
Phase: N/A
Study type: Observational [Patient Registry]

The registry aims to evaluate the safety, performance and efficacy of the Everolimus-eluting bioresorbable vascular scaffold (BVS) system following rotational atherectomy in patients with complex de novo native coronary artery lesions in all-day clinical practice.

NCT ID: NCT01824030 Recruiting - Clinical trials for Ischemic Heart Disease

FFR or OCT Guidance to RevasculariZe Intermediate Coronary Stenosis Using Angioplasty

FORZA
Start date: April 2013
Phase: Phase 3
Study type: Interventional

Whether to revascularize patients with angiographically-intermediate coronary lesions (AICL) is a major clinical issue. Intravascular techniques (assessing either the anatomy or the functional effect of coronary stenoses) are routinely used to better characterize coronary lesions. Among these,fractional flow reserve (FFR) provides validated functional insights while optical coherence tomography (OCT) provides high resolution anatomic imaging. Both techniques may be applied to guide decisions regarding the opportunity to revascularize patients with AICL and to optimize the result of percutaneous coronary intervention (PCI). We aim to compare the clinical and the economical impact of FFR versus OCT guidance in the percutaneous management of patients with AICL.