跳至主要内容
临床试验/NCT02752191
NCT02752191已完成4 期

Feraheme As An MRI Contrast Agent For Pediatric Congenital Heart Disease

Paul Finn1 个研究点 分布在 1 个国家目标入组 17 人开始时间: 2016年4月最近更新:
适应症
干预措施

试验速览

阶段
4 期
状态
已完成
发起方
入组人数
17
试验地点
1
主要终点
Composite Image Quality Score Among 7 Anatomical Structures.

研究概览

简要总结

The standard clinical cardiovascular MRI practice for children with CHD frequently involves the use of gadolinium-based contrast agents (GBCA) to enhance tissue contrast. Most GBCAs are small molecules that quickly cross the capillary wall and access the interstitial space, a process which diminishes the signal contrast between blood vessels and surrounding tissue. Therefore, these types of GBCA are most useful for first-pass MR angiography, wherein the images are acquired quickly during the initial 15-30 seconds post-injection when the GBCA concentration is much higher in the arteries than in the interstitial space. For young children with complex CHD, the stringent requirements for high spatial resolution, and the need for cardiac gating and good blood-myocardium contrast in order to provide detailed evaluation of intracardiac structures are not compatible with conventional GBCA-based first-pass MR angiography. Even with Ablavar® (gadofosveset trisodium), an FDA approved GBCA with longer intravascular half-life than other GBCAs, cardiac-gated Ablavar®-enhanced MRI may be insufficient for young children with CHD based on our institutional experience and on data from the literature; there remains diminished blood-tissue contrast during the high-resolution cardiac-gated MRI. Furthermore, there have been safety concerns regarding gadolinium deposition in brain tissues after repeated GBCA exposure as well as concerns of nephrogenic systemic fibrosis (NSF) associated with GBCA injection in young children < 2 years old who may have immature renal function. The long-term health consequences of these effects in the pediatric population are unclear. For the above reasons, we seek to study the diagnostic imaging effectiveness of Feraheme (Feraheme®), an FDA-approved drug for parenteral iron supplementation, as an MRI contrast agent in children with CHD. Although Feraheme® has been approved for the treatment of iron deficiency anemia secondary to renal disease, Feraheme® has been used as an off-label MRI contrast agent at select medical centers.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Other
盲法
None

入排标准

年龄范围
1 Day 至 6 Years(Child)
性别
All
接受健康志愿者

入选标准

  • Male or female pediatric patients of all ethnicities (age newborn to 6 years) with known or suspected CHD with inconclusive echocardiographic exams and are referred for cardiovascular MRI for further evaluation of cardiac anatomy and function.
  • Written informed consent obtained from subject's legal representative/guardian(s) and ability for subject to comply with the requirements of the study

排除标准

  • Standard clinical contraindications to MRI, including subjects with cochlear implants and implanted cardiac devices
  • Subjects with past or current diagnosis of iron overload due to hereditary hemochromatosis or other causes (for subjects receiving Feraheme injection only).
  • Subjects with known hypersensitivity or allergy to iron oxide particles.
  • Subjects with renal insufficiency defined as estimated glomerular filtration rate (eGFR) < 40 mL/min/1.73m2 (for subjects receiving Ablavar injection only).
  • Subjects who are critically ill at the time of MRI and for whom the period of general anesthesia and separation from the critical care nursery or intensive care unit poses added risk as deemed by referring cardiologists, cardiac surgeons or the managing radiologist (for Part II only).
  • Other medical conditions, in the judgment of the clinician investigator, that would increase the risks to the child related to participation in the study.

研究组 & 干预措施

Ferumoxytol

Active Comparator

Ferumoxytol, 4mg/kg of body weight, one time infusion of several minutes

干预措施: ferumoxytol (Drug)

gadofosveset

Active Comparator

gadofosveset, 0.03mmol/kg, one time bolus injection

干预措施: gadofosveset (Drug)

结局指标

主要结局

Composite Image Quality Score Among 7 Anatomical Structures.

时间窗: day 1

1-4 image quality Likert score by an imaging expert, with 4 representing excellent image quality and 1 is non-diagnostic

次要结局

  • Incidence of Adverse Events(day 1)
  • Image Quality Score at Individual Anatomical Sites.(day 1)

研究者

发起方
Paul Finn
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Paul Finn

Professor

University of California, Los Angeles

研究点 (1)

Loading locations...

相似试验

Feraheme As An MRI Contrast Agent For Pediatric... | 临床试验