Actively Recruiting

Phase Not Applicable
Age: 18Years - 85Years
All Genders
NCT02723500

129 Xenon MRI in Chronic Lung Disease

Led by Western University, Canada · Updated on 2024-06-13

100

Participants Needed

1

Research Sites

748 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Subjects aged 18-85 with lung disease will undergo hyperpolarized Xenon 129 (129-Xe) MRI and Pulmonary Function testing for the development of tools to evaluate the Apparent Diffusion Coefficient (ADC), ventilation defect percent (VDP) and pulmonary gas exchange measurements obtained by analysis of hyperpolarized 129-Xe MRI.

CONDITIONS

Official Title

129 Xenon MRI in Chronic Lung Disease

Who Can Participate

Age: 18Years - 85Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults aged 18 to 85 years with diagnosed lung disease including asthma, emphysema, COPD, bronchiectasis, sarcoidosis, pulmonary fibrosis, alpha 1-anti-trypsin deficiency, or lymphangioleiomyomatosis (LAM)
  • Willingness to participate and provide written informed consent
  • Ability to hold breath for 16 seconds
  • Judged to be in stable health based on medical history
  • Able to perform reproducible pulmonary function testing with acceptable spirometry results
  • Forced Expiratory Volume at one second (FEV1) greater than 25% predicted
  • Forced Vital Capacity (FVC) greater than 25% predicted and greater than 0.5 liter
Not Eligible

You will not qualify if you...

  • Mentally or legally incapacitated individuals unable to provide informed consent or understand written material
  • Daytime room air oxygen saturation less than or equal to 92% while lying down
  • Unable to perform spirometry or plethysmography tests
  • Unable to tolerate MRI due to body size or claustrophobia
  • Pregnant or lactating individuals
  • Physical or psychological conditions preventing MRI performance, such as severe claustrophobia
  • Presence of MRI incompatible devices or non-removable metal in the body such as pacemakers, neurostimulators, insulin pumps, aneurysm clips, bioprosthesis, metallic fragments, shunts, surgical staples, or ear implants

AI-Screening

AI-Powered Screening

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Trial Site Locations

Total: 1 location

1

Robarts Research Institute; The University of Western Ontario; London Health Sciences Centre

London, Ontario, Canada, N6A 5B7

Actively Recruiting

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Research Team

G

Grace E Parraga, PhD

CONTACT

A

Angela P Wilson, RRT

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

BASIC_SCIENCE

Number of Arms

1

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