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临床试验/NCT01165892
NCT01165892已完成不适用

Pulmonary MR Angiography and Lower Extremity MR Venous Imaging Using a Single Dose of Gadofosveset (Ablavar)

Washington University School of Medicine0 个研究点目标入组 15 人开始时间: 2011年7月最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
15
主要终点
Imaging Outcome

研究概览

简要总结

The use of the contrast agent, Ablavar, will help with the diagnosis of pulmonary embolism in magnetic resonance imaging (MRI).

详细描述

Specific Aim 1: To assess first-pass SNR and CNR of pulmonary MR angiography performed with 0.03 mmol/Kg of intravenous gadofosveset trisodium.

Hypothesis: Use of 0.03 mmol/Kg of gadofosveset trisodium in gradient recalled echo pulmonary MR angiography will provide a pulmonary artery SNR and CNR equal to or better than the SNR and CNR obtained using the same MR technique with 0.2 mmol/Kg of a conventional contrast agent (gadopentetate dimeglumine) and equal to or better than 0.1 mmol/Kg of intravenous gadobenate dimeglumine. Data will be compared to SNR and CNR of pulmonary MR angiogram images obtained at Washington University as part of the PIOPED III study.

Specific Aim 2: To assess SNR and CNR of breath-hold pulmonary MR imaging obtained immediately after the original first-pass breath-hold pulmonary MR angiography.

Hypothesis: SNR and CNR of pulmonary MR angiography performed immediately after first-pass breath-hold pulmonary MR angiography will be at least equal to the SNR and CNR obtained using the same MR technique with 0.2 mmol/Kg of a conventional contrast agent (gadopentetate dimeglumine) and at least equal to 0.1 mmol/Kg of intravenous gadobenate dimeglumine.

Specific Aim 3: To assess SNR and CNR of lower extremity MR venogram (MRV) performed immediately after the two pulmonary MR angiograms, described above.

研究设计

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

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patient that have pulmonary embolism.
  • 18 yrs of age and older

排除标准

  • allergy to gadolinium based contrast.
  • allergy to iodated based contrast.
  • renal insufficiency (GFR < 60 mL/min?1.73m2)
  • pregnant or nursing
  • contraindication to MRI

结局指标

主要结局

Imaging Outcome

时间窗: Upon imaging

Assessment of imaging parameters such as SNR, CNR

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

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