Clinical Trials Logo

Heart Valve Diseases clinical trials

View clinical trials related to Heart Valve Diseases.

Filter by:

NCT ID: NCT02574650 Recruiting - Heart Valve Disease Clinical Trials

Early Feasibility of the Mitralign Percutaneous Tricuspid Valve Annuloplasty System (PTVAS) Also Known as TriAlign™.

SCOUT
Start date: November 2015
Phase: N/A
Study type: Interventional

The purpose of this study is to assess the early safety and performance of the Mitralign Percutaneous Tricuspid Valve Annuloplasty System (PTVAS) for the treatment of symptomatic chronic functional tricuspid regurgitation (FTR). The procedure will be performed with the PTVAS device using a non-surgical percutaneous approach to tricuspid valve repair in patients who have FTR with a minimum of moderate tricuspid regurgitation.

NCT ID: NCT02518282 Recruiting - Clinical trials for Myocardial Infarction

High-sensitivity Troponin T in Acute Myocardial Infarction After Cardiac Valvular Surgery

Start date: January 2014
Phase: N/A
Study type: Observational

A measurable degree of heart muscle tissue injury is expected in patients undergoing heart valvular surgery. The level of this injury can be measured by cardiac biomarkers in blood samples. Those biomarkers are used to diagnose an acute myocardial infarction. Postoperative myocardial infarction (MI) is a frequent and important complication after cardiac surgery with high morbidity and mortality. Therefore it is very important to recognize any cardiac event in patients who undergo cardiac surgery. Different diagnostic tools can be used to the diagnosis of acute myocardial infarction; however few is known about the value of high-sensitivity cardiac troponin T (hs-cTn) to diagnose a MI after heart valvular surgery. The aim of this study is to determine the upper reference limit of high-sensitivity troponin T concentration to consider the diagnosis of acute myocardial infarction in patients undergoing heart valvular surgery.

NCT ID: NCT02515539 Recruiting - Clinical trials for Cardiovascular Disease

Early Feasibility Study of the CardiAQ™ TMVI System (Transfemoral and Transapical DS)

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

The purpose of the study is to generate early US feasibility data of the CardiAQ™ Transcatheter Mitral Valve Implant System. The study will enroll patients with moderate to severe mitral valve regurgitation who are considered high risk for mortality and morbidity from conventional open-heart surgery.

NCT ID: NCT02478008 Recruiting - Clinical trials for Cardiovascular Disease

A Clinical Study of the CardiAQ™ TMVI System (Transapical DS)

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

The purpose of the study is to evaluate the initial short and long-term safety and performance of the CardiAQ™ Transcatheter Mitral Valve Implantation System using the Transapical Delivery System. The study will enroll patients with moderate to severe mitral valve regurgitation who are considered high or extreme risk for mortality and morbidity from conventional open heart surgery.

NCT ID: NCT02400125 Recruiting - Clinical trials for Coronary Artery Bypass Grafting

China Cardiovascular Surgery Registry

CCSR
Start date: March 2013
Phase: N/A
Study type: Observational [Patient Registry]

China Cardiovascular Surgery Registry (CCSR) Study is a national database for coronary artery bypass grafting (CABG) and valve surgery performed in 87 hospitals with cardiovascular surgery volume > 100 per year. The aims of CCSR Study are: (i) report the characteristics of patient, the quality and evolvement of CABG and valve procedures in China, (ii) build and valid surgical risk assessment tools for Chinese population, (iii) provide databases for clinical studies, and quality improvement initiatives.

NCT ID: NCT02219984 Recruiting - Atrial Fibrillation Clinical Trials

START-Register: Survey on Anticoagulated Patients Register

Start date: October 2011
Phase:
Study type: Observational [Patient Registry]

This is a phase 4 cohort prospective, open, national, multicentre study that collects data on history of patients treated chronically with anticoagulant drugs, including the novel direct oral anticoagulants (DOACs). The Registry is designed solely for observational purposes and is not intended to have any influence on the treatment of the single patients included. Patients are included when they start the anticoagulant treatment, whatever the drug used, or when they shift from a vitamin K antagonist (VKA) drug to one of the novel direct oral anticoagulants, provided that the therapy is expected to last at least 3 months. The general aims of the study are to provide a better evaluation of efficacy and safety of different treatment options, and to improve our understanding of the risks/benefits of the various anticoagulant drugs and the different therapy options. The Registry is open to the participation of clinical centres or individual professionals (now called Participants) that are involved with management of anticoagulated patients.

NCT ID: NCT02173860 Recruiting - Clinical trials for Coronary Artery Disease

Strategies for Revascularization in Patients Undergoing Heart Valve Surgery With Concomitant Coronary Artery Disease

SAVE-IT
Start date: July 2016
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether, in patients undergoing elective valvular heart surgery, revascularization of concomitant coronary artery disease (CAD) guided by FFR (Fractional flow reserve) would be superior to standard angiography-guided-revascularization approach on major efficacy and safety outcomes

NCT ID: NCT02003885 Recruiting - Clinical trials for Valvular Heart Disease

Effect of Desflurane on Cardiac Function During Cardiac Surgery: Tissue Doppler Imaging of Mitral Valve Annular Velocity

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

The purpose of this study is to determine desflurane's dose-dependent effect on left ventricular (LV) function in cardiac surgery. The change of tissue Doppler imaging (TDI) of lateral mitral valve annular velocity at three different desflurane concentrations would be analyzed by using intraoperative transesophageal echocardiography (TEE) in cardiac surgery patients

NCT ID: NCT01906918 Recruiting - Clinical trials for Coronary Artery Disease

Application of Remote Ischemic Preconditioning in Patients Undergoing Open Heart Surgeries

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

Strategies for myocardial protection during open heart surgeries are desired. Several experimental studies have shown beneficial effects of remote ischemic preconditioning (RIPC). The underlying mechanisms are not totally understood. This study intends to evaluate molecular mechanisms involved with RIPC on myocardium of patients underwent open heart surgeries.

NCT ID: NCT01855737 Recruiting - Atrial Fibrillation Clinical Trials

The Study of Warfarin Maintenance Dose in Chinese Patients

WADCH
Start date: June 2013
Phase: Phase 4
Study type: Observational

1. Title: Clinical study of the relationship between Pharmacogenomics and warfarin dose in Chinese patients 2. Drug: Warfarin 3. Design: To value the accuracy of warfarin Pharmacogenomics algorithm by the algorithm calculated dose and actual dose in the Chinese patients. 4. Hypothesis:Pharmacogenomic algorithm guided dose can help to predict warfarin dose in Chinese patients.