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临床试验/NCT02431598
NCT02431598已完成4 期

Randomized, Blinded, Placebo-controlled Crossover Study Assessing Association Between Gadolinium-based Contrast Agent Administration and Transient Dyspnea/Arterial Phase Motion Artifact

Duke University1 个研究点 分布在 1 个国家目标入组 44 人开始时间: 2015年6月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
已完成
入组人数
44
试验地点
1
主要终点
Subject Breath Hold Capacity, as Measured by Number of Seconds a Subject Can Hold His/Her Breath

研究概览

简要总结

The purpose of this study is to evaluate changes in volunteer breath-holding capacity in response to gadoxetate disodium (Eovist) administration, compared with saline, and gadoterate dimeglumine (Dotarem). Healthy volunteers will be recruited from three study sites. These subjects will be given three, blinded, randomized injections while undergoing an MRI of their liver and holding their breath. During the scan, the subjects' oxygen saturation and heart rate will be closely monitored. Following the scan, the subjects will complete a questionnaire regarding the breath hold.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Diagnostic
盲法
Single (Participant)

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • normal renal function (serum eGFR >60)

排除标准

  • renal impairment
  • allergy to gadolinium-based contrast
  • metallic implanted devices
  • claustrophobia
  • pregnant and lactating females

研究组 & 干预措施

Eovist (gadoxetate disodium)

Active Comparator

While in the MRI scanner, the subject will receive a clinical dose of Eovist, Dotarem, or normal saline. Each subject will receive all three, in random order, blinded to which agent is received in a given instance.

干预措施: gadoxetate disodium (Drug)

Dotarem (gadoterate dimeglumine)

Active Comparator

While in the MRI scanner, the subject will receive a clinical dose of Eovist, Dotarem, or normal saline. Each subject will receive all three, in random order, blinded to which agent is received in a given instance.

干预措施: gadoterate dimeglumine (Drug)

Saline

Active Comparator

While in the MRI scanner, the subject will receive a clinical dose of Eovist, Dotarem, or normal saline. Each subject will receive all three, in random order, blinded to which agent is received in a given instance.

干预措施: Saline (Drug)

结局指标

主要结局

Subject Breath Hold Capacity, as Measured by Number of Seconds a Subject Can Hold His/Her Breath

时间窗: following contrast administration, up to 5 minutes

Subject-reported Dyspnea, as Measured by Questionnaire Responses

时间窗: following contrast administration, up to 5 minutes

After each breath-hold, the MRI technologist asked the volunteer through the scanner microphone the following two questions, with responses based on a 5-point scale: A) How difficult was it to hold your breath? (1-Not at all; 5-Very difficult); B) Do you feel short of breath now? (1-Not at all; 5-Very short of breath). Responses were recorded for each breath-hold.

次要结局

  • O2 Saturation Following Contrast Administration(following contrast administration, up to 5 minutes)
  • Heart Rate Following Contrast Injection(following contrast administration, up to 5 minutes)
  • Severity of Motion Artifacts at Arterial Phase Imaging, Measured on a 1-5 Scale(following contrast administration, up to 5 minutes)
  • Percentage of Participants With Transient Severe Motion (TSM) Based on Presence of Motion Artifacts at Arterial Phase Imaging(following contrast administration, up to 5 minutes)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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