MagniXene MRI Use in Patients With Asthma and COPD to Assess Regional Lung Function by Delineating Ventilation Defects
Completed · Phase 2
Conditions studied: Asthma, COPD, Healthy
In brief
The purpose of this clinical trial is to demonstrate hyperpolarized xenon (HXe) as a medical imaging drug (agent) for Magnetic Resonance Imaging (MRI) of the human lung ventilation.
Key facts
- Study ID
- NCT01833390
- Run by
- Xemed LLC
- People needed
- 58
- Starts
- 2011-09-01
- Expected to finish
- 2015-01-01
- Last updated by the study team
- 2015-03-11
Who can join
Age: 21 and older, up to 75. Sex: any. Healthy volunteers: accepted.
You may not qualify if…
- Baseline oxygen requirement.
- Blood oxygen saturation of 92% less than as measured by pulse oximetry on the day of imaging.
- FEV1 percent predicted less than 25%.
- Pregnancy or lactation.
- Claustrophobia, inner ear implants, aneurysm or other surgical clips, metal foreign bodies in eye, pacemaker or other contraindication to MR scanning. Subjects with any implanted device that cannot be verified as MRI compliant will be excluded.
- Chest circumference greater than that of the xenon MR coil.
- History of congenital cardiac disease, chronic renal failure, or cirrhosis.
- Inability to understand simple instructions or to hold still for approximately 10 seconds.
- History of respiratory infection within 2 weeks prior to the MR scan.
- History of heart attack, stroke and/or poorly controlled hypertension.
- Known hypersensitivity to albuterol or any of its components, or levalbuterol.
Where it is running
- University of Virginia — Charlottesville, Virginia, United States
Full record on ClinicalTrials.gov
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