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Kawasaki Disease clinical trials

View clinical trials related to Kawasaki Disease.

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NCT ID: NCT01524939 Completed - Kawasaki Disease Clinical Trials

Study of Combined Therapy of Aspirin and "IVIG-SN" in Kawasaki Disease

Start date: January 2012
Phase: Phase 4
Study type: Interventional

The purpose of this study is to evaluate the safety, efficacy and of Immune Globulin Intravenous (Human) IVIG-SN™ in subjects with kawasaki diseases.

NCT ID: NCT01440075 Completed - Kawasaki Disease Clinical Trials

Prevalence and Early Markers of Atherosclerosis in Adults With a History of Kawasaki Disease

Kawasaki
Start date: October 10, 2011
Phase: N/A
Study type: Interventional

Kawasaki disease (KD) is an acute systemic vasculitic syndrome with coronary tropism. It has been reported worldwide, but it is ten times more common in Asian population. The annual incidence in children under 5 years in Europe is estimated at 8 to 100000. It is the second vasculitis of the child by its frequency after rheumatoid purpura. It occurs in 80% of cases between 1 and 5 years, with a maximal incidence around the age of 12 months. It may results in acquired heart disease in children in developed countries, and may be the cause of premature coronary artery disease in adulthood. A polymorphism was recently associated with the occurrence of disease in a Japanese and U.S population. (C allele of SNP itpkc_3, with a risk multiplied by 2). However, data are conflicting on this issue and the prevalence of this allel is unknown in North America and Europe populations. The clinical picture of KD associate a persistent fever and an antipyretics resistance with mucocutaneous signs and bulky cervical lymphadenopathy usually unilateral. Diagnosis is confirmed by the presence of five clinical signs (major criteria). The presence of inconsistent coronary lesions in cardiac ultrasound can confirm the diagnosis. KD can resolve spontaneously with no treatment. The severity of the disease is primarily related to complications of coronary aneurysms in acute or chronic stages. Several arguments support the fact that adult patients have diffuse vascular lesions different from aneurysmal lesions initially described in childhood. Despite abundance of publications on KD, there is no prospective or retrospective study which explored anomalies resulting from KD in adult subjects. Therefore, this project will describe the patient's vascular evolution, the prevalence of atherosclerotic lesions and to determine the biological and functional abnormalities, markers of accelerated atherosclerosis. Hypothesis : A history of Kawasaki disease represents a cardiovascular risk factor in adulthood. The main objective is to evaluate the prevalence of atherosclerotic lesions, their extent and their severity in adults with a history of KD in childhood compared to a control population.

NCT ID: NCT01431105 Completed - Kawasaki Disease Clinical Trials

Pharmacokinetics (PK)/Safety Study of Atorvastatin in Children With Kawasaki Disease and Coronary Artery Abnormalities

Start date: July 2012
Phase: Phase 1/Phase 2
Study type: Interventional

Kawasaki disease (KD) is the leading cause of acquired heart disease in children in the developed world. Despite available treatment, 25% of children in San Diego County appropriately treated for KD develop coronary artery abnormalities that could lead to complications later in life, including heart attack. Although investigators can identify children with KD that have these coronary artery abnormalities, there is no approved additional treatment to decrease coronary artery inflammation and arrest or prevent damage to the coronary arteries. Inflammation and damage to the arterial wall is central to these coronary artery abnormalities. Statins, a class of drugs that is known for lowering cholesterol, have also been shown to decrease inflammation in general as well as at the level of the vessel wall. Therefore, the investigators propose to study the safety of the drug atorvastatin in children with coronary artery abnormalities from KD.

NCT ID: NCT00861848 Completed - Heart Disease Clinical Trials

Real Time Myocardial Contrast Echocardiography and Dobutamine Stress Perfusion Magnetic Resonance Imaging

ECHOBIKE
Start date: April 1, 2009
Phase:
Study type: Observational

The present study is designed to: 1. investigate the safety and efficacy of Real time myocardial echocardiography (RT-MCE) in adolescents and adults ages 12-50 with congenital and acquired congenital heart disease 2. compare RT-MCE with dobutamine stress perfusion MR for determination of coronary flow reserve and ventricular wall motion 3. assess regional myocardial mechanics using myocardial speckle tracking and MR tagging. 4. evaluate RV volume and function for a subset of subjects using novel reconstruction software

NCT ID: NCT00841789 Completed - Kawasaki Disease Clinical Trials

A Randomized, Double Blind, Placebo Controlled Study of Etanercept in Children With Kawasaki Disease

Start date: March 2009
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine whether Etanercept (Enbrel) when used in conjunction with IVIG and aspirin, improves treatment response to IVIG in patients with Kawasaki Disease. Funding Source- FDA/OOPD

NCT ID: NCT00760435 Completed - Kawasaki Disease Clinical Trials

Infliximab Plus Intravenous Immunoglobulin for the Primary Treatment of Kawasaki Disease

Start date: March 2009
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine whether the addition of infliximab to standard primary therapy of intravenous immunoglobulin (IVIG) and high dose aspirin will reduce resistance to therapy in acute Kawasaki disease (KD).

NCT ID: NCT00271570 Completed - Kawasaki Disease Clinical Trials

Infliximab (Remicade) for Patients With Acute Kawasaki Disease

Start date: April 2004
Phase: Phase 1
Study type: Interventional

This study evaluates the safety of infliximab in infants and children with acute Kawasaki Disease.

NCT ID: NCT00162045 Completed - Kawasaki Disease Clinical Trials

A Trial to Determine Radiation Exposure to Organs and Assess the Safety of CARDIOLITE® in Pediatric Subjects

Start date: January 2005
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this Phase I-II multicenter clinical trial is to establish dosimetry and safety profiles for CARDIOLITE® (Technetium Tc99m Sestamibi) in pediatric subjects.

NCT ID: NCT00162032 Completed - Kawasaki Disease Clinical Trials

A Study to Evaluate the Use and Safety of CARDIOLITE® in Pediatric Patients With Kawasaki Disease

Start date: August 2005
Phase: Phase 3
Study type: Interventional

Determine the predictive value of CARDIOLITE® rest and stress myocardial perfusion imaging (MPI) to define a pediatric population with Kawasaki Disease (KD) at high and low risk of developing cardiac events.