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临床试验/NCT02892136
NCT02892136进行中(未招募)不适用

Technical Development for Pediatric Cardiovascular MRI

Children's National Research Institute1 个研究点 分布在 1 个国家目标入组 5,000 人开始时间: 2013年5月最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
发起方
入组人数
5,000
试验地点
1
主要终点
To evaluate innovative noninvasive MRI techniques suitable for evaluating pediatric patients with cardiovascular disease, congenital cardiac disease, and fetal organ analysis including cardiac structure, function, and physiology.

研究概览

简要总结

This study will explore new ways of using magnetic resonance imaging (MRI) to evaluate pediatric patients with cardiovascular disease,congenital heart disease in patients of all ages, fetuses undergoing clinically indicated MR imaging.

详细描述

The purpose of this protocol is to allow development and testing of new MRI techniques suitable for evaluating patients with cardiovascular disease, congenital heart disease, fetal cardiac structure, function, and physiology, and other fetal organ analysis. Individuals referred to Children's National Medical Center for a clinically indicated cardiac MRI or cardiac catheterization by their primary referring cardiologist or obstetrician, and who are enrolled in this study may also undergo additional research imaging.

Since such technical development work often depends on preliminary studies in healthy volunteers, the protocol also recruits healthy subjects.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

性别
All
接受健康志愿者

入选标准

  • Clinically indicated exams
  • Patients who are undergoing a medically indicated MRI scan or cardiac catheterization procedure
  • Patients who are medically judged to have no contraindications to MRI scan
  • Age inclusion: infant to adult
  • Written informed consent and assent, when applicable
  • Written informed consent from any normal volunteer 8 years of age or older for a noncontrast, nonsedated cardiac MRI
  • Normal adult volunteer to undergo cardiac MRI with contrast agent
  • Fetal exams
  • Age inclusion:18 years and older
  • Second or third trimester (greater than 13 weeks)

排除标准

  • All patients who are medically judged to have contraindication(s) to MRI scanning will be excluded. Contraindications include implanted metal devices which are contraindicated for MRI scanning:
  • Central nervous system aneurysm clips;
  • Implanted neural stimulator;
  • Implanted cardiac pacemaker or defibrillator;
  • Cochlear implant;
  • Ocular foreign body (e.g. metal shavings);
  • Implanted Insulin pump;
  • Metal shrapnel or bullet.
  • Exclusion criteria for Bicycle Stress MRI
  • Myocardial infarction within 24 hours
  • Active myocarditis
  • Uncontrolled heart failure
  • Severe left ventricular outflow tract obstruction
  • Exclusion Criteria for adult volunteers undergoing MRI with administration of contrast agent:
  • 60 years of age or older
  • Renal Disease; Glomerular Filtration rate (eGFR < 30 ml/min/1.73 m2) will be determined by a simple blood test done at the bedside
  • Use of diuretics
  • Diagnosis of hypertension and diabetes
  • Exclusion criteria for volunteers undergoing both contrast and non-contrast
  • Pregnant women:
  • Women of childbearing potential will be required to have a screening urine pregnancy test
  • Exclusion criteria for
  • Pregnant woman for whom 15 additional minutes lying flat in the MR scanner would represent a risk (i.e. severe claustrophobia, congestive heart failure)
  • Pregnant minor under the age of 18
  • Less than 13 weeks gestation

结局指标

主要结局

To evaluate innovative noninvasive MRI techniques suitable for evaluating pediatric patients with cardiovascular disease, congenital cardiac disease, and fetal organ analysis including cardiac structure, function, and physiology.

时间窗: through study completion, an average of 1 year

次要结局

  • Natural history of congenital heart disease(through study completion, an average of 1 year)

研究者

发起方
Children's National Research Institute
申办方类型
Other
责任方
Principal Investigator
主要研究者

Russell Cross

MD

Children's National Research Institute

研究点 (1)

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