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Congenital Heart Disease Clinical Trials

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

RESULTS

Found (41) clinical trials

People with congenital heart defects are asked to participate in a research study being conducted by Montefiore Medical Center.

Phase N/A

Post-market Clinical Follow-up Study With Magnetic Resonance Imaging Conditional Guide Wire

This is post-market clinical follow-up study on 25 consecutive patients in two centers to evaluate the safety of a guide wire conditional for use in magnetic resonance imaging and the acceptability of identified risks in the clinical evaluation and to detect emerging risks on the basis of factorial evidence. The ...

Phase N/A

Aortic Replacement Using Individualised Regenerative Allografts - ARISE (the "Surveillance")

This is a prospective, non-randomized, single-arm, multi-centre surveillance study to be conducted in Europe. The Surveillance is designed as a study, where - ARISE AV is prescribed in the usual manner in accordance with the terms of the approval. - Assignment of the patient to a particular therapeutic strategy is ...

Phase N/A

Percutaneous Closure of Atrial Septal Defects in Children: Integration of 3D Echocardiography and Fluoroscopy Imaging.

The software "Echonavigator" will be used after the introduction of the percutaneous closure of ASD prosthesis. The image fusion on fluoroscopy will then be applied and the bias between the generated ultrasound image and the X-ray view of the prosthesis will be measured. The center marker visible prosthesis ultrasound and ...

Phase N/A

Evaluation of Safety and Efficacy of Lumason in Pediatric Echocardiography

This is a Phase III, multicenter, open-label study that will be conducted at approximately 7-12 sites in the United States, Canada and Europe in pediatric patients with suboptimal LV EBD on non-contrast 2D transthoracic echocardiography with harmonic imaging. It is estimated that 92 patients will be enrolled to provide 73 ...

Phase

Lifetech CeraFlex Post-Market Surveillance Study

The Lifetech CeraFlex devices are CE marked and shall be used in this study within its intended use as described in the approved corresponding Instructions For Use (IFU). Approximately 120 patients will be included in this study. The patient population will consist of 40 consecutive patients with a confirmed secundum ...

Phase N/A

Fontan Udenafil Exercise Longitudinal Assessment Trial

This study is a randomized, double-blinded, efficacy trial of the effects of udenafil vs. placebo on the background of standard therapy on maximal VO2 (ml/kg/min) from baseline to six months in adolescent survivors of the Fontan procedure. . The target sample size is 400 subjects (200 per group).

Phase