Evaluation of Ventilation Defects Downstream of Mucus Plugs in Patients With Muco-Obstructive Lung Disease
Recruiting
Observational Study
Severe AsthmaCOPDNon-CF BronchiectasisCystic Fibrosis (CF)
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
No Study Drug
Researchers observe your health over time — no experimental treatment is given.
Ready to participate?
Review the details below, then apply to join this clinical trial.
At a Glance
Age
18 – 65
Sex
Any
Study type
Observational
Participants needed
8 (estimated)
Sponsor
University of Kansas Medical Center · Other
Who this trial is looking for
This trial is looking for patients with muco-obstructive lung diseases like COPD or cystic fibrosis. Participants will have MRIs to assess how mucus plugs affect breathing in their lungs.
Are You a Good Fit for This Trial?
You may be able to join if
I am between 18 and 65 years old.
I have been diagnosed with muco-obstructive pulmonary disease for more than 1 year.
I can complete the informed consent process.
I can perform a breathing test (spirometry) as needed.
You may not be able to join if
I have had a respiratory infection in the last 4 weeks.
My body mass index (BMI) is more than 30.
I have visited the emergency room for my lung condition in the past 4 weeks.
I have a significant medical illness like heart disease or cancer.
My resting oxygen level is below 90%.
I am pregnant or have a positive pregnancy test.
I have participated in another clinical trial within the last 30 days.
Summarized in plain language from this trial's official eligibility criteria.
The full criteria are further down this page — only the research team can
confirm whether you qualify.
Think this trial could be right for you?
Answer a few quick questions to see if you may meet the eligibility requirements.
In this study, xenon MRI will be used to evaluate regional functional consequences of mucus plugs in the lungs of patients with muco-obstructive pulmonary disease. Mucus plugs will be identified using CT imaging, and xenon MRI will be used to evaluate ventilation and gas exchange impairments in regions of the lungs corresponding to the airways downstream of mucus plugs.
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Adequate completion of informed consent process with written documentation
* Patients 18 - 65 years old
* • Physician diagnosis of muco-obstructive pulmonary disease, including cystic fibrosis, severe asthma, chronic obstructive pulmonary disease, or non-cystic fibrosis bronch…
Inclusion Criteria:
* Adequate completion of informed consent process with written documentation
* Patients 18 - 65 years old
* • Physician diagnosis of muco-obstructive pulmonary disease, including cystic fibrosis, severe asthma, chronic obstructive pulmonary disease, or non-cystic fibrosis bronchiectasis for \> 1 year
* Able to perform reproducible spirometry according to ATS criteria based on clinical PFTs.
Exclusion Criteria:
* Respiratory tract infection within the 4 weeks prior to Visit 1
* Body mass index (BMI) \> 30 at Visit 1
* One-time doses such as intra-articular injections require a 4-week washout prior to Visit 1
* ER visit related to pulmonary condition within the previous 4 weeks of Visit 1
* Significant concomitant medical illness, including (but not limited to) heart disease, cancer, uncontrolled diabetes, other chronic lung diseases (determined by the Investigator.)
* Resting O2 saturation \<90% with maximum supplemental O2 delivered by nasal canula
* Positive urine pregnancy test
* Participation in an intervention study (including bronchoscopy) or use of investigative drugs within the past 30 days or plans to enroll in such a trial during the study
* Unable or unlikely to complete study assessments in the opinion of the Investigator
* Study intervention poses undue risk to patient in the opinion of the Investigator
* Conditions that will prohibit MRI scanning determined by the MRI safety screening.
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