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Aortic Stenosis clinical trials

View clinical trials related to Aortic Stenosis.

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NCT ID: NCT01966146 Completed - Aortic Stenosis Clinical Trials

Examination of Valve Insufficiency Before and After MitraClip or TAVI Procedure by 3D Echocardiography Compared to MRI

3D_TTE_TAVI
Start date: May 2013
Phase: N/A
Study type: Interventional

Aim of the study is the definition of criteria for a standardized assessment of heart function by 3D echocardiographic procedures. Standardized criteria will be defined to assess aortic valve insufficiency after TAVI and success of mitral valve replacement respectively.

NCT ID: NCT01941420 Completed - Aortic Stenosis Clinical Trials

Comparison of Blood and Crystalloid Cardioplegia

Start date: November 2006
Phase: N/A
Study type: Observational [Patient Registry]

The investigators decided to make a study with a cohort of patients as homogenous as possible with a cross clamp time around 70 min. Adult patients with a severe aortic stenoses without any other significant heart disease was included in our prospective randomised study. This group of patients was chosen for two reasons. First, these patients have left ventricular hypertrophy making the myocardium vulnerable to ischemia, secondly the investigators wanted to avoid the possible confounding effect of ischemia found in patients with variable degrees of coronary artery disease. Therefore, patients with additional significant coronary artery disease (≥ 50% stenoses) were excluded from the study.

NCT ID: NCT01876420 Completed - Aortic Stenosis Clinical Trials

The Medtronic CoreValve™ Evolut R™ CE Mark Clinical Study

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

To assess the safety and clinical performance of the CoreValve™ Evolut R™ System.

NCT ID: NCT01845207 Completed - Aortic Stenosis Clinical Trials

Frailty Assessment Before Cardiac Surgery & Transcatheter Interventions

Start date: January 2012
Phase: N/A
Study type: Observational [Patient Registry]

Frailty is a state of decreased physiologic reserves and vulnerability to stressors. Several tools exist to measure frailty, some based on physical tests and others on questionnaires, yet there is no agreement on which tool to recommend. This multi-center prospective cohort study is aimed at comparing various frailty assessment tools to determine which best predicts death or major complications after cardiac surgery or transcatheter intervention. The population of interest is elderly patients with severe aortic stenosis undergoing surgical or transcatheter aortic valve replacement. The frailty assessment tools under investigation include composite frailty scales, physical performance tests, muscle mass, and biomarker expression. The overall objective is to improve our ability to predict risk by measuring frailty using the optimal tool in elderly cardiovascular patients.

NCT ID: NCT01837160 Completed - Aortic Stenosis Clinical Trials

Angiogenesis and Fibrosis in Aortic Stenosis

Start date: April 2013
Phase: N/A
Study type: Observational

Angiogenesis and fibrosis lie at the heart of a number of fundamental processes responsible for cardiovascular disease. In this proposal, the investigators intend to build upon a highly successful programme of studies exploring the cardiovascular applications of positron emission tomography. Specifically, the investigators will explore the potential role of a novel radiotracer, 18F-fluciclatide, which is a highly selective ligand for the αvβ3 and αvβ5 integrin receptors that are up regulated during angiogenesis, and tissue fibrosis and remodelling. This tracer has been successfully used to assess angiogenesis in metastatic tumours and its uptake is suppressed by anti-angiogenic therapies. The investigators here propose to describe the pattern of uptake of 18F-fluciclatide in cardiovascular diseases, specifically aortic stenosis and aortic atherosclerosis. The investigators will correlate 18F-fluciclatide uptake with in vivo measures of angiogenesis and fibrosis as well as ex vivo histological characterisation of tissue. If successful, this novel radiotracer could provide an extremely important non-invasive method of assessing in vivo angiogenesis, plaque vulnerability, and tissue remodelling as well as potential applications in developing stem cell therapies.

NCT ID: NCT01755936 Completed - Aortic Stenosis Clinical Trials

The Role of Myocardial Fibrosis in Patients With Aortic Stenosis

Start date: January 2012
Phase:
Study type: Observational

Aortic stenosis is the most common adult valvular heart disease in the western world. Heart failure and sudden cardiac death are complications associated with aortic stenosis. In symptomatic individuals, valve replacement is often the only effective treatment. However, there are no good markers to identify patients who may benefit from early surgery before symptoms developed. The purpose of the study is to test the hypothesis that the presence heart muscle scarring on the cardiac magnetic resonance imaging may predict a worse outcome in patients with aortic stenosis, and thus may be helpful in identifying patients for early valve replacement.

NCT ID: NCT01755338 Completed - Aortic Stenosis Clinical Trials

Effect of Steroids on Cerebral Inflammation and Neuronal Damage After Surgical Aortic Valve Replacement

Start date: December 2012
Phase: N/A
Study type: Interventional

The purpose of this study is to investigate if methylprednisolone is effective in reducing the cerebral inflammatory response after open heart surgery with cardiopulmonary bypass.

NCT ID: NCT01736956 Completed - Aortic Stenosis Clinical Trials

Fetal Intervention for Aortic Stenosis and Evolving Hypoplastic Left Heart Syndrome

Start date: October 2012
Phase: N/A
Study type: Interventional

For fetuses with severe aortic stenosis, in utero balloon aortic valvuloplasty may improve fetal growth of left heart structures and thus improve potential for biventricular repair strategies after birth.

NCT ID: NCT01676727 Completed - Aortic Stenosis Clinical Trials

ADVANCE Direct Aortic Study

Start date: September 2012
Phase:
Study type: Observational

This study is intended to collect data regarding the clinical utility, safety and performance of the Medtronic CoreValve® System for Transcatheter Aortic Valve Implantation (TAVI) in patients with severe symptomatic aortic valve stenosis for which treatment via direct aortic access (DA) is selected.

NCT ID: NCT01672268 Completed - Aortic Stenosis Clinical Trials

Interest of Cardiac Computed Tomography to Optimize and Improve the Procedure of TAVI

CT-TAVI
Start date: February 2012
Phase: Phase 3
Study type: Interventional

This is a pilot prospective, comparative, monocentric, randomized study with 2 groups. People with a severe aortic stenosis and a high risk of surgery are referred to a Trans catheter aortic valve implantation (TAVI).