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Vascular Diseases Clinical Trials

A listing of Vascular Diseases medical research trials actively recruiting patient volunteers. Search for closest city to find more detailed information on a research study in your area.

Found 147 clinical trials

Resuscitation Registry in CHD

Children with congenital heart defects are far more likely to suffer a cardiovascular arrest and be in the need of cardiopulmonary resuscitation than healthy children or those with diseases of other organ systems, especially after cardiothoracic surgery. Due to a lack of data, the exact number of resuscitations in this …

- 18 years of age Both Phase N/A

MRI to Predict Rejection and Failure in Transplant and Cardiomyopathy Patients

Overall Research Strategy of this protocol is to refine and validate noninvasive CMR imaging sequences with invasive hemodynamic and pathology results to create a comprehensive, noninvasive, radiation-reduced regimen for pediatric cardiomyopathy and cardiac transplant assessment. We were the first to perform MR-guided cardiac catheterization in US children, and have accumulated …

6 - 100 years of age Both Phase N/A
M Magalie LADOUCEUR, MD, PHD

Gender Difference in NET Activation in Patients With Congenital Heart Disease and Heart Failure

Neutrophil hyperactivation has detrimental effects on cardiac tissue after injuries, leading to fibrosis lesions and cardiac dysfunction. It is now well-established that women present with different clinical symptoms in cardiovascular disease compared to men. A cardioprotective effect in women has been suggested in some studies including patients with congenital heart …

18 - 45 years of age Both Phase N/A
C Christoph Gräni, MD PhD

European Prospective Registry on Anomalous Aortic Origin of the Coronary Arteries

Anomalous aortic origin of a coronary artery (AAOCA) is a group of rare congenital heart defects with various clinical presentations. The lifetime-risk of an individual living with AAOCA is unknown, and data from multicentre registries are urgently needed to adapt current recommendations and guide optimal patient management. The European Registry …

- 100 years of age Both Phase N/A
V Victor Waldmann

French National Registry of Patients With Tetralogy of Fallot and Implantable Cardioverter Defibrillator

National french registry of patients with tetralogy of Fallot and implantable cardioverter defibrillator.

18 - 100 years of age Both Phase N/A
E Edward O'Leary, MD

Atrial Late Gadolinium Enhancement in Patients With Repaired Congenital Heart Disease

In this research study the investigators want to learn more about how well the investigators can visualize scar tissue in the heart by MRI. In patients with congenital heart disease who need a procedure in the electrophysiology laboratory, how the MRI findings match the findings in the electrophysiology laboratory is …

13 - 100 years of age Both Phase N/A
S Shoujun Li, MD

The Follow-up System of Pediatric Heart Failure and the Establishment of End-stage Heart Failure Registry

Establish a follow-up management system for pediatric heart failure and a registration platform for end-stage heart failure

- 14 years of age Both Phase N/A
A ACHD Research Team

Pathophysiologic Mechanism for Arrhythmias and Impaired Aerobic Capacity in Tetralogy of Fallot and Other Congenital Heart Diseases

This study is being done to determine the mechanism(s) contributing to the onset of symptoms (i.e. shortness of breath and/or palpitations) as well as changes in heart structure in patients with congenital heart disease (CHD)

18 - 100 years of age Both Phase N/A
F Francesco Bianco, M.D.

Repaired Tetralogy of Fallot Italian Registry

The CMR/CT WG of the Italian pediatric cardiology society set up a multi-center observational clinical database of repaired-TOF evaluated. This registry will enroll prospectively patients evaluated by CMR for clinical indication in most of the CHD Italian centers. Data collection will include surgical history, clinical data, imaging data, and also …

10 - 100 years of age Both Phase N/A
A AURIOL Françoise

Constitution of a Biological Collection to Study the Pathophysiology in Noonan Syndrome

The present study will establish a collection of biological samples from Noonan patients to be used for research purposes only, with due respect for confidentiality.

18 - 99 years of age Both Phase N/A

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