Hyperpolarized Xenon-129 Lung Magnetic Resonance Imaging: Healthy Adult Volunteer Pilot Study

Sponsor
The Hospital for Sick Children (Other)
Overall Status
Recruiting
CT.gov ID
NCT02195206
Collaborator
(none)
32
1
96
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Study Details

Study Description

Brief Summary

In this pilot study, MRI of the lungs of healthy adult volunteers will be performed at 3Tesla to assess image quality using a prototype chest coil and pulse sequence following inhalation of hyperpolarized 129Xe (xenon) gas. This study will take place at the Hospital for Sick Children, Toronto, Canada. Thirty two subjects aged 18 to 75 will participate in this study. Xenon MRI is a non-invasive imaging technique that does not involve X-rays or ionizing radiation. Rather, this imaging method utilizes the same hardware and software principles that are used for conventional proton MRI of patients in a hospital. The investigators are testing the abilities of xenon MRI to see if it will produce lung images of equal or better quality to that of proton MRI.

The investigators hypothesize that they will get good quality images of the lungs for analysis using our method.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    With the emergence of novel hardware and software image acquisition improvements, magnetic resonance imaging (MRI) has the potential to become an important tool for assessing lung structure and function. In particular, the use of a hyperpolarized noble gas such as 129Xe has been used to explore structural and functional relationships in the lungs of both healthy subjects and patients with lung disease (1,2). In contrast to proton-based MRI imaging, 129Xe gas is used as a "contrast agent" to directly visualize the airways, and thus image ventilation. Whereas the normal density of gas is too low to produce an easily detectable signal, this is overcome by artificially increasing the amount of polarization per unit volume using optical pumping (3).

    Hyperpolarized noble gas MR lung imaging is a relatively new imaging method that allows depiction of both lung function and morphology [4-9]. Hyperpolarized gases are a new class of MR contrast agent which, when inhaled, provide high temporal and spatial resolution MR images of the lung airspaces. Since no ionizing radiation is involved, hyperpolarized gas MR imaging is ideal for the evaluation of lung diseases. With hyperpolarized gases, the nuclear spins of the gas atoms are brought into alignment outside of the MR scanner via a process called optical pumping; this yields high polarizations and permits visualization of the lung airspaces with MR imaging (despite the low physical density of the gas in the lung). Two non-radioactive (i.e. stable) isotopes of noble gases 3He and 129Xe can be hyperpolarized. Until recently, higher polarizations could be achieved with 3He than with 129Xe, so in humans, 3He was more commonly used for hyperpolarized gas MR imaging of the lungs [10-15]. Recently, the technology has been developed to provide large quantities of highly polarized 129Xe [16].

    Several applications of 129Xe MRI imaging are under development, including diffusion-weighted and relaxation-weighted imaging (17-19). These techniques take advantage of the fact that the rate of loss of 129Xe polarization is significantly influenced by the local blood flow and concentration of molecular oxygen, as well as the restriction of 129Xe diffusion by small airway space dimensions. These data can be used to create maps of the lung reflecting regional ventilation/perfusion and micro-airway sizes. Other data that can be obtained with 129Xe MRI include the volumes of ventilated and unventilated lungs which can subsequently be analyzed to determine the homogeneity of gas distribution within the airspaces (17).

    Objectives of the study are:
    • To quantitatively evaluate a 3T 129Xe chest coil for image quality and coil comfort/performance.

    • To determine the range of possible novel pulse sequences in combination with the coil and inhalation of 129Xe gas in healthy volunteers.

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    32 participants
    Observational Model:
    Case-Only
    Time Perspective:
    Cross-Sectional
    Official Title:
    Development of Hyperpolarized Xenon-129 Lung Magnetic Resonance Imaging Hardware and Software: Healthy Adult Volunteer Pilot Study
    Study Start Date :
    Jul 1, 2014
    Anticipated Primary Completion Date :
    Jul 1, 2022
    Anticipated Study Completion Date :
    Jul 1, 2022

    Arms and Interventions

    Arm Intervention/Treatment
    Healthy

    Adult

    Outcome Measures

    Primary Outcome Measures

    1. Ventilation Defect Volume [Day 1]

      Volume of the lung not being ventilated to the optimum level

    Secondary Outcome Measures

    1. Apparent Diffusion Coefficient [Day 1]

      Used to obtain structural information of the lung. Metric for assessing tissue damage.

    Other Outcome Measures

    1. Signal to Noise Ratio [Day 1]

      Used to assess image quality

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 75 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • Subjects male and female aged 18-75

    • Subject has a smoking history of ≤ 1 pack year

    • Subject understands the study procedures and is willing to participate in the study as indicated by signature on the informed consent

    • Subject must be able to perform a breath hold for 16 seconds

    • Subject has a Body Mass Index (BMI) between 18 and 40

    • Subject is judged to be in stable health on the basis of medical history

    • Subject able to perform reproducible pulmonary function tests (i.e., the 3 best acceptable spirograms have Forced Expiratory Volume (FEV1) values that do not vary more than 5% of the largest value or more than 100 ml, whichever is greater)

    Exclusion Criteria:
    • Subject is, in the opinion of the investigator, mentally or legally incapacitated, preventing informed consent from being obtained, or cannot read or understand the written material

    • Subject has a history of chronic or acute respiratory disease

    • Subject has a history of cardiovascular disorders including coronary insufficiency, cardiac arrhythmias, severe hypertension (≥160 over ≥100)

    • Subject has a daytime room air oxygen saturation ≤ 92% ± 2% while supine

    • Subject is unable to perform spirometry or plethysmography maneuvers

    • Subject is pregnant or lactating

    • In the investigator's opinion, subject suffers from any physical, psychological or other condition(s) that might prevent performance of the MRI, such as severe claustrophobia

    • Subject has an MRI incompatible device or any metal in their body which cannot be removed, including but not limited to pacemakers, neurostimulators, biostimulators, implanted insulin pumps, aneurysm clips, bioprosthesis, artificial limb, metallic fragment or foreign body, shunt, surgical staples (including clips or metallic sutures and/or ear implants)

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 The Hospital for Sick Children Toronto Ontario Canada M5G 1X8

    Sponsors and Collaborators

    • The Hospital for Sick Children

    Investigators

    • Principal Investigator: Giles Santyr, PhD, The Hospital for Sick Children

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Giles Santyr, PhD, FCCPM, Senior Scientist, The Hospital for Sick Children, The Hospital for Sick Children
    ClinicalTrials.gov Identifier:
    NCT02195206
    Other Study ID Numbers:
    • 1000041669
    First Posted:
    Jul 21, 2014
    Last Update Posted:
    Aug 18, 2021
    Last Verified:
    Aug 1, 2021
    Keywords provided by Giles Santyr, PhD, FCCPM, Senior Scientist, The Hospital for Sick Children, The Hospital for Sick Children

    Study Results

    No Results Posted as of Aug 18, 2021