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Active clinical trials for "Aortic Valve Stenosis"

Results 531-540 of 802

Percutaneous Aortic Valve 18F System for the Treatment of Patients With Severe Aortic Stenosis

Aortic Valve Stenosis

The purpose of the study is to determine the safety and performance of the Direct Flow Medical study valve and delivery procedure.

Unknown status42 enrollment criteria

Ultrasonic Markers for Myocardial Fibrosis and Prognosis in Aortic Stenosis

Aortic Valve StenosisMyocardial Fibrosis

This study is part of a research project in which new ultrasound-based techniques will be examined to improve clinical decision making for patients with aortic stenosis. These patients could develop increased amounts of myocardial fibrosis. This fibrosis is associated with the patients' prognosis. Fibrosis can be evaluated with magnetic resonance imaging (MRI), which unfortunately is quite expensive and not easily available. Ultrasound-based parameters will be developed for the assessment of the amounts of myocardial fibrosis, especially in the left ventricle. Then it will be examined whether these parameters can predict the patients magnitude of fibrosis and check for association with the patients prognosis. MRI will serve as a gold standard for quantification of myocardial fibrosis. The new echocardiographic techniques and parameters are expected to provide new insights in the interplay between aortic stenosis and left ventricular function, and to ultimately improve the care for patients with aortic stenosis. The present study's objectives are: Quantify the level of myocardial fibrosis in mild, moderate, and severe aortic stenosis compared with a healthy population. Evaluate the patients outcome after one and three year of follow-up

Completed10 enrollment criteria

Comparison of Carbon Dioxide and Saline Flush to Saline Flush in TEVAR and TAVI Procedures to Reduce...

Thoracic Aortic AneurysmAortic Stenosis Symptomatic2 more

Thoracic endovascular repair (TEVAR) and transcatheter aortic valve implantation (TAVI) are standard of care procedures to treat thoracic aortic aneurysm or severe aortic stenosis, respectively. Both procedures have a high risk of stroke and silent infarction. Gas has been detected in the cerebral vasculature during these procedures and associated with DWI positive lesions on MRI. The hypothesis is that air emboli contribute to stroke and silent infarction. The investigators propose addressing air emboli by flushing the device with carbon dioxide prior to flushing with saline. This is a pilot study comparing standard saline flush alone to carbon dioxide flushing with saline flush.

Unknown status14 enrollment criteria

Elimination of CO2-insufflation-induced Hypercarbia in Open Heart Surgery

Adult Patients Undergoing Open Heart Replacement of the Aortic Valve for Aortic Stenosis or Insufficiency

The study aim was to evaluate if an additional separate venous reservoir eliminates CO2-insufflation induced hypercapnia and keeps sweep gas flow of the oxygenator constant during open heart surgery.

Unknown status3 enrollment criteria

Conduction Disease After Transcatheter Aortic Valve Replacement

Aortic StenosisHeart Block1 more

This is a prospective single center Cardiology department observational study. The study aim is to better understand the predictors of high grade conduction abnormalities associated with TAVR such that a more robust evidence-based and universal strategy to manage cardiac conduction disturbances in these patients, which has been elusive, can be developed.

Completed5 enrollment criteria

Use of Virtual Reality for Procedural Planning of Transcatheter Aortic Valve Replacement

Aortic StenosisSevere

This study sought to evaluate the impact of Virtual Reality (VR) tools in procedural planning of transcatheter aortic valve replacement (TAVR).

Completed2 enrollment criteria

Transcatheter Aortic Valve Replacement System Pivotal Trial

Aortic Valve Stenosis

Prospective, randomized, unblinded, multi-center investigational study with enrollment at up to 45 investigational sites. The study is designed to compare the study device (Direct Flow Medical Transcatheter Aortic Valve System) composite event rate to a blended commercial comparator (using approved Medtronic self-expanding bioprosthesis or Edwards balloon-expandable bioprosthesis) in high and extreme risk Subjects with severe symptomatic aortic stenosis. Subjects will be followed through the index procedure, hospital discharge, and at 30 days, 6 months and 1 year for the primary endpoint analysis. Thereafter, annual follow-up at 2 through 5 years will be conducted and analyzed separately.

Unknown status35 enrollment criteria

Examination of Valve Insufficiency Before and After MitraClip or TAVI Procedure by 3D Echocardiography...

Development of Standardized Assessment TAVI and MitraClip Procedures by EchocardiographyAortic Stenosis1 more

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.

Completed12 enrollment criteria

Statin Therapy in Asymptomatic Aortic Stenosis

Aortic Valve Stenosis

There is evidence that the degenerative changes leading to aortic stenosis are caused by a chronic inflammatory process. Furthermore the development of aortic stenosis is partially dependent on typical cardiovascular risk factors. An inflammatory process as well as those risk factors are amenable for medical therapy. As such the use of statins (HMG CoA reductase inhibitors) would be an appealing concept to reduce both those risks for development of aortic stenosis. Aim of this study is to evaluate the usefulness of statin therapy on the progression of aortic stenosis.

Unknown status20 enrollment criteria

Evaluating the Risk of Cognitive Impairment After Surgical and Transcatheter Aortic Valve Replacement...

Cardiovascular DiseaseAortic Valve Stenosis4 more

The investigators are conducting a pilot study to compare cognitive outcomes among Veterans with severe aortic valve stenosis who are scheduled to undergo either aortic valve replacement.

Completed4 enrollment criteria
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