Clinical Trials Logo

Aortic Valve Stenosis clinical trials

View clinical trials related to Aortic Valve Stenosis.

Filter by:

NCT ID: NCT01775215 Withdrawn - Aortic Stenosis Clinical Trials

A Comparison of Advanced Imaging Techniques in Aortic Stenosis

AIm-AS
Start date: January 2013
Phase: N/A
Study type: Observational

In patients with aortic stenosis the valve through which blood is pumped out of the main heart chamber is narrowed. This results in heart muscle working harder to open the valve so blood can circulate around the body. The muscle adapts to the increased pressure load to maintain efficiency. This can cause long-term muscle damage. To predict when this deterioration will require a valve replacement is difficult and untimely operation exposes patients to unnecessary risk. We aim to compare all validated techniques looking at different aspects of heart muscle strain in these patients. These will be a blood sample measuring a specific hormone (BNP) and enzyme (Troponin), a nuclear scan to assess nerve activation, an MRI identifying scarring and an exercise echocardiogram that measures heart muscle response and pressure changes across the valve. Tests will be performed at recruitment and either after one year or after valve replacement, which ever comes first. In comparing these different imaging techniques we aim to identify patients who will benefit from an early operation, those whose muscle is likely to recover back to normal and which patients it is safe to wait longer for the surgery, avoiding unnecessary risk. The results of the study will benefit patients as it will help doctors more accurately assess the timing of valve surgery and improve their prediction of long term heart muscle recovery. It may also increase convenience in clinical management by reducing unnecessary tests and hospital trips. This would translate into cost savings for the NHS.

NCT ID: NCT01742598 Withdrawn - Clinical trials for Severe Symptomatic Aortic Stenosis

Assessment of St Jude Medical Portico Re-sheathable Transapical Aortic Valve System

Portico TA EU
Start date: December 2015
Phase: N/A
Study type: Interventional

The purpose of this study is to assess the safety and performance of the 23mm Portico Transcatheter Heart Valve and the TAVI Transapical Delivery System in subjects with severe symptomatic aortic stenosis

NCT ID: NCT01648309 Withdrawn - Aortic Stenosis Clinical Trials

Neuropsychological Testing in Patients Undergoing Transvascular Aortic Valve Implantation

TAVIPSYCH
Start date: September 2012
Phase: N/A
Study type: Observational

The purpose of this study is to examine the neuropsychological effects of transvascular aortic valve implantation (TAVI). Patients undergoing TAVI usually suffer from congestive heart failure and low cardiac output which may limit their cognitive abilities. TAVI results in significant improvements in cardiac function and therefore may improve cognitive functions. However, TAVI may also be associated with stroke and may therefore have a negative impact on cognition. Therefore, in this study the investigators wish to perform a battery of standardized neuropsychological tests before and after TAVI to test the net effects of TAVI on cognitive performance over time. The investigators plan to include all patients planned to have TAVI in the study and to test them before, 3,7, 30 and 360 days post TAVI with a standardized battery of test.

NCT ID: NCT00774657 Withdrawn - Aortic Stenosis Clinical Trials

Ventricular Remodeling In Patients With Aortic Stenosis Assessed Echocardiography

Start date: September 2008
Phase: N/A
Study type: Observational

This preliminary study will compare the effectiveness of two-dimensional and three-dimensional echocardiographic measurements of wall thickness and left ventricular mass in patients with Aortic Stenosis

NCT ID: NCT00618293 Withdrawn - Clinical trials for Blood Loss, Surgical

Haemate HS in Patients With Severe Bleeding Undergoing Valve Replacement Due to Aortic Stenosis

HAVAS
Start date: January 2008
Phase: Phase 2
Study type: Interventional

Evaluation of efficacy by determination of transfusion requirements and safety by determination of adverse events in administration of Von Willebrand factor concentrate F VIII (Haemate).

NCT ID: NCT00598754 Withdrawn - Clinical trials for Aortic Valve Stenosis

Diagnostic Three Dimensional Echocardiography Study Protocol

Start date: June 2001
Phase: N/A
Study type: Observational

The purpose of this study is to perform ground-based research to study what happens to the heart muscle in space. People who have problems with their aortic valve have an increase in the amount of muscle in the left ventricle of the heart. After valve surgery, the amount of muscle should decrease and return to normal. Astronauts lose heart muscle mass during space flight. Our study will look at these changes in your heart, which we believe are similar to what happens during long term space travel. This study will look at the accuracy of three dimensional ultrasound imaging (echo) in monitoring the changes in heart size and function following aortic valve replacement. We are studying ways to prevent health-related problems that men and women will face on long-duration space missions. The hypothesis is that serial two dimensional and three dimensional echo will show accurate changes in the left ventricle mass and volume following aortic valve replacement for aortic stenosis or regurgitation