Last updated: November 2, 2020
Sponsor: University of Virginia
Overall Status: Active - Recruiting
Phase
1/2
Condition
N/ATreatment
N/AClinical Study ID
NCT03331302
20053
Ages > 18 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- Subjects must have a diagnosis of COPD
- at their clinical baseline on the day of imaging
- must be clinically stable in order to participate in the study.
- COPD subjects will be categorized according to the GOLD
- Current/Former SmokerSubjects
- must have a smoking history ≥ 10 pack years
Exclusion
Exclusion Criteria:
- Dx of asthma
- Continuous oxygen use at home
- Blood oxygen saturation of 92% less than as measured by pulse oximetry on the day ofimaging
- FEV1 percent predicted less than 25%
- Pregnancy or lactation
- Claustrophobia, inner ear implants, aneurysm or other surgical clips, metal foreignbodies in eye, pacemaker or other contraindication to MR scanning
- Subjects with any implanted device that cannot be verified as MRI compliant will beexcluded
- Chest circumference greater than that of the xenon MR and/or helium coil. Thecircumference of the coil is approximately 42 inches
- History of congenital cardiac disease, chronic renal failure, or cirrhosis
- Inability to understand simple instructions or to hold still for approximately 10seconds
- History of respiratory infection within 2 weeks prior to the MR scan
- History of MI, stroke and/or poorly controlled hypertension.
Study Design
Total Participants: 30
Study Start date:
September 01, 2018
Estimated Completion Date:
December 31, 2020
Study Description
Connect with a study center
University of Virginia Health System
Charlottesville, Virginia 22908
United StatesActive - Recruiting
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