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临床试验/NCT02019251
NCT02019251已完成1 期

Evaluation of Regional Lung Function in Lung Transplant Recipients Using 19F Magnetic Resonance Imaging of Inert Perfluorinated Gases Mixed With Oxygen

Hal C Charles1 个研究点 分布在 1 个国家目标入组 6 人开始时间: 2013年12月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
1 期
状态
已完成
发起方
入组人数
6
试验地点
1
主要终点
obtain regional, non-invasive images of pulmonary function in patient's post lung transplantation

研究概览

简要总结

The goal of this study is to evaluate the utilization of conventional 'thermally' polarized perfluorinated gases mixed with oxygen as inhaled inert contrast agents to image the airway spaces in subjects who have undergone single or double lung transplantation. This is an open label study expanding on current work here at Duke. Images will be obtained using 19F MRI during wash-in and washout for evaluation of ventilation efficiency.

详细描述

This is an open label study in up to 10 lung transplant recipients post lung transplantation whose post-transplant status is being monitored according to local standard of care. Each subject will receive up to 20 liters of PFP/oxygen gas mixtures as a contrast agent to visualize the airway and alveolar spaces in their lungs using 19F magnetic resonance imaging of inert gas/oxygen mixtures.

The goal of this study is to evaluate the utilization of conventional 'thermally' polarized perfluorinated gases mixed with oxygen as an exogenous inert contrast agent to image the airway spaces in subjects with transplanted lungs. This is an open label proof of concept study expanding on work here at Duke.

The central hypothesis and current observation is that PFx gases, when used as contrast agents, provide functional images of the lung airways including important regional ventilation information such as ventilation defect severity and gas trapping. We will test the central hypothesis and accomplish the overall objective by addressing the following specific aims:

Primary Study Aims/Secondary Aims Aim 1: Determine qualitative and quantitative measures of lung ventilation performance in terms of ventilation efficiency during wash-in evaluation of the 19F images of lung airspaces.

Aim 2: Determine qualitative and quantitative measures of lung ventilation performance in terms of direct measures of gas trapping measured during washout of the perfluorinated gas mixture.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Diagnostic
盲法
None

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

  • Subjects must meet all of the following inclusion criteria to be eligible for enrollment into the trial:
  • Subjects must be ≥ 18 years of age;
  • Post single or double lung transplant;
  • Subjects who are willing and able to comply with scheduled visits and other trial procedures

排除标准

  • Subjects presenting with any of the following will not be included in the trial:
  • Unable to undergo a 3.0-Tesla MRI exam of the lungs and chest because of contraindications (e.g. metal in the eye, claustrophobia);
  • Unable to receive gas mixture by breathing because of contraindications;
  • Participation in a clinical trial with a study drug that may impact lung function in the past 14 days; or
  • Other severe acute or chronic medical or psychiatric condition or laboratory abnormality that may increase the risk associated with trial participation or may interfere with the interpretation of trial results and, in the judgment of the investigator, would make the subject inappropriate for entry into this trial.
  • Female; women at risk of pregnancy are required to have a confirmed negative blood pregnancy test at Screening if of childbearing potential prior to the MRI scan.

研究组 & 干预措施

Post single or double lung transplant

Experimental

The subjects will receive the gas by breathing perfluorinated gas/oxygen mixture using Disposable Face mask and a standard Douglas Bag system.

干预措施: perfluorinated gas/oxygen mixture (Drug)

Post single or double lung transplant

Experimental

The subjects will receive the gas by breathing perfluorinated gas/oxygen mixture using Disposable Face mask and a standard Douglas Bag system.

干预措施: MRI (Device)

结局指标

主要结局

obtain regional, non-invasive images of pulmonary function in patient's post lung transplantation

时间窗: 1 day (Single exposure)

次要结局

未报告次要终点

研究者

发起方
Hal C Charles
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Hal C Charles

Associate Professor Department of Radiology

Duke University

研究点 (1)

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