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Heart Valve Diseases clinical trials

View clinical trials related to Heart Valve Diseases.

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NCT ID: NCT04126018 Recruiting - Aortic Stenosis Clinical Trials

Comparative Imaging Assessment of Valvular Heart Disease

Start date: August 23, 2019
Phase:
Study type: Observational

The purpose of the study is to compare the various 2D and 3D methods of valvular heart disease quantification (Doppler, PISA, VCA, volumetric method) and strain with cardiac magnetic resonance (CMR) measurements of left and right ventricular systolic function strain and myocardial fibrosis assessment.

NCT ID: NCT04080219 Recruiting - Clinical trials for Valvular Heart Disease

The Impact of Sleep-disordered Breathing on the Incidence of Postoperative Acute Kidney Injury in Patients Undergoing Valvular Heart Surgery

Start date: December 19, 2018
Phase:
Study type: Observational

Sleep-disordered breathing has a prevalence of 30~80% in patients with heart diseases. Various studies have revealed a correlation between the incidence and various diseases such as heart failure, hypertension, diabetes, and cerebral infarction. Postoperative acute kidney injury after heart surgery is one of the major complications with incidence with 40~50%, however, there has been no preventive method or treatment yet. Recently, several studies have been published that have shown a correlation between sleep-disordered breathing and renal impairment. In general, sleep-disordered breathing can be regulated easily with continues positive expiratory pressure, which means that early diagnosis and treatment of sleep-disordered breathing might help to reduce the incidence of postoperative acute kidney injury and improve patients' prognosis. In this study, the investigators investigate the impact of sleep-disordered breathing (diagnosed by oxygen desaturation index ≥5) on the incidence of postoperative acute kidney injury in patients undergoing valvular heart surgery.

NCT ID: NCT04073420 Recruiting - Clinical trials for Valve Disease, Heart

Medtronic Cardiac Surgery PMCF Registry

Start date: December 2, 2019
Phase:
Study type: Observational [Patient Registry]

This registry is being conducted to support ongoing post-market surveillance activities.

NCT ID: NCT04047082 Recruiting - Clinical trials for Heart Valve Diseases

Online Videodensitometric Assessment of Aortic Regurgitation in the Cath-Lab

OVAL
Start date: May 15, 2019
Phase:
Study type: Observational [Patient Registry]

Following the high feasibility of analyses by core laboratory with videodensitometry determined in the ASSESS-REGURGE Registry, this is an early clinical feasibility study of online videodensitometric assessment of aortograms to quantitate aortic regurgitation (AR) in the cath lab, specifically in the setting of transcatheter aortic valve replacement (TAVR)

NCT ID: NCT04031144 Recruiting - Clinical trials for Cardiac Valve Disease

Ultrafiltration on Coagulation Function in Cardiac Surgery

Start date: January 30, 2020
Phase: N/A
Study type: Interventional

To determine the effect of modified ultrafiltration, which is usually employed for reducing free water at the end of cardiopulmonary bypass (CPB), on coagulation profile in patients undergoing cardiac surgery

NCT ID: NCT04015973 Recruiting - Clinical trials for Coronary Artery Disease

The PRE-OP ENERGY Trial

Start date: May 7, 2019
Phase: N/A
Study type: Interventional

The PRE-OP ENERGY Trial proposes to test the overarching hypothesis that a pre-surgery high energy diet will protect patients against organ damage during cardiac surgery with cardiopulmonary bypass.

NCT ID: NCT04011501 Recruiting - Pain, Postoperative Clinical Trials

Erector Spinae Plane Block for Minimal Invasive Cardiac Surgery (Heart-Port).

ESP
Start date: May 7, 2019
Phase: N/A
Study type: Interventional

Minimally invasive cardiac surgery is performed through a right thoracotomy, the pain management of this surgery is of great importance. Regional techniques such as thoracic epidural anesthesia or paravertebral block are excellent techniques for the management of postoperative pain in thoracic surgery but they have disadvantages that make it difficult to use in this surgery. On the one hand, anticoagulation in these patients increases the risk of complications related to the use of neuraxial techniques and, on the other hand, the technical difficulty of paravertebral block. The erector of the spine block is a technically simple block and with a low risk of associated complications. The aim of the study is to evaluate the feasibility and benefits in the relationship of postoperative pain management in patients undergoing minimally invasive cardiac surgery when using continuous unilateral blockade of the erector in a small cohort of patients.

NCT ID: NCT03977129 Recruiting - Clinical trials for Primary Valvular Heart Disease With Comorbid Coronary Artery Disease

Quantitative Flow Ratio (QFR) Guided Revascularization Strategy for Patients Undergoing Primary Valve Surgery With Comorbid Coronary Artery Disease

FAVOR4-QVAS
Start date: August 4, 2019
Phase: N/A
Study type: Interventional

This is a multicenter, prospective, randomized, blinded, controlled clinical study in patients with planned primary valvular surgery and comorbid coronary artery lesions with diameter stenosis of ≥ 50%, to compare the effectiveness of an Quantitative Flow Ratio (QFR)-guided revascularization strategy and a coronary angiography (CAG)-guided revascularization strategy in preventing the incidence of composite outcome (MACE-5, including all-cause death, myocardial infarction, stroke, unplanned coronary revascularization, and new renal failure requiring dialysis) within 30 days after surgery. The study hypothesis is that the QFR-guided strategy can reduce the incidence of the MACE-5 within 30 days after surgery, as compared with the CAG-guided strategy.

NCT ID: NCT03885180 Recruiting - Valve Heart Disease Clinical Trials

Randomized Evaluation of D-dimer Guiding dUration of Oral antiCoagulation thErapy

REDUCE
Start date: March 20, 2019
Phase: N/A
Study type: Interventional

Guidelines recommended that patients with bioprosthetic heart valves (BHV) only need 6 months oral anticoagulation therapy after operation. However, a small part of patients still suffered thrombotic events after withdrawal of warfarin, which means these patients may need extend anticoagulation therapy. D-dimer, a sensitive marker of thrombosis or prethromboembolism state. Previous studies have demostrated that patients with elevated D-dimer levels have significant more clinical outcomes than those with nagative D-dimer levels. The aim of this study was to evaluate whether D-dimer could guide the duration of oral anticoagulation therapy in patients with BHV.

NCT ID: NCT03840928 Recruiting - Obesity Clinical Trials

PatientSpot Formerly Known as ArthritisPower

Start date: April 1, 2015
Phase:
Study type: Observational [Patient Registry]

Patient Power is a patient research network and database (registry) to collect prospective information about demographics, self-reported diagnoses and medications, and willingness to participate in research from participants with rheumatoid arthritis (RA), spondyloarthritis (SpA), other musculoskeletal conditions, chronic neurological conditions like migraine, chronic pulmonary conditions like Chronic Obstructive Pulmonary Disease (COPD), asthma, autoimmune dermatological conditions such as psoriasis, and other chronic inflammatory or immune-mediated conditions. In addition, since patients with chronic conditions often have other co-morbidities like cardiovascular health and obesity-related metabolic disorders, these conditions will also be included. Participants will provide information from their smartphones or personal computers. The information will be used by researchers and clinicians to help patients and their providers make better, more informed decisions about treatment of chronic conditions.