Fact CheckerSign in

NCT06057714Recruiting

Quantitation and Spatial Registration of Airways Dysfunction With Dynamic 19F MRI in Cystic Fibrosis

Source: ClinicalTrials.gov · Last updated 2 Jul 2026

Brief summary (registry, in English)

The purpose of this study is to look at lung ventilation in people with cystic fibrosis over time (1 year) using magnetic resonance imaging (MRI) with an inhaled contrast gas, and compare these measures to lung function assessed by spirometry and multiple breath nitrogen washout. This study also looks at how these measures change in response to a pulmonary exacerbation and treatment (if applicable). Over the span of a year, participants would be asked to complete 3-5 visits to the University of North Carolina at Chapel Hill (UNC). with each lasting up to 4 hours. If participants do not have a pulmonary exacerbation during the year they would be asked to complete 3 visits (one at enrollment, a second roughly 2 weeks later, and the third approximately a year later). If participants do experience a CF pulmonary exacerbation they would complete 5 visits (Visit 1, Visit 2, two exacerbation visits with one before treatment and the other after, and Visit 3 at one year after Visit 1). Only one exacerbation per participant will be tracked. Participants are eligible for this study if they are 18 years old or older, have Cystic Fibrosis (CF) with mild lung disease (FEV1 \>/= 60%), and can undergo an MRI. There are no known benefits for participating in this study.

Status (registry)
Recruiting
Study type
Observational
Enrollment
30 (estimated)
First submitted
18 Sept 2023
Start date
Jan 2021
Primary completion date
Aug 2026
Lead sponsor
University of North Carolina, Chapel Hill
NCT number
NCT06057714

What you commit to

  • Study type: Observational
  • Planned participants: 30
  • From Jan 2021 to the primary completion date, Aug 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Presence of facial hair that may interfere with the fit of the mask (and unwillingness to shave prior to each MRI)
  • Pregnancy; women of childbearing potential must have a confirmed negative urine pregnancy test on the day of the MR scan, prior to the MRI scan.

Other illness

  • Any changes in medications that may affect CF lung disease in the past 28 days, including any experimental therapies

Lab values

  • Other severe acute or chronic medical or psychiatric condition or laboratory abnormality that may increase the risk associated with trial participation or may interfere with the interpretation of trial results and, in the judgment of the investigator, would make the subject inappropriate for entry into this trial.

Age

  • Unable to undergo a 3.0-Tesla MRI exam of the lungs and chest because of contraindications including
    • Occupation (past or present) of machinist, welder, or grinder;
    • Injury to the eye involving a metallic object
    • Injury to the body by a metallic object (bullet, bullet ball, shrapnel)
    • Presence of a cardiac pacemaker or defibrillator
    • Presence of aneurysm clips
    • Presence of carotid artery vascular clamp
    • Presence of neurostimulator
    • Presence of insulin or infusion pump
    • Presence of implanted drug infusion device that is not known to be MRI compatible (i.e., was placed outside of UNC or is older than 10 years)
    • Bone growth or fusion simulator
    • Presence of cochlear, otologic or ear implant
    • Any type of prosthesis (eye, penile, etc.)
    • Artificial limb or joint
    • Non-removable electrodes (on body, head or brain)
    • Intravascular stents, filters or coils
    • Shunt (spinal or intraventricular)
    • Swan-Ganz catheter
    • Any implant held in place by a magnet
    • Transdermal delivery system (e.g. Nitro)
    • An intrauterine device or diaphragm that is not MRI compatible
    • Tattooed makeup (eyeliner, lips, etc.) or tattoos covering \>25% of body surface area
    • Body piercings (must be removed before MRI)
    • Any metal fragments
    • Internal pacing wires
    • Metal or wire mesh implants
    • Hearing aid (remove before MRI) aa. Dentures (remove before MRI) bb. Claustrophobia

Other

  • Subjects presenting with any of the following will not be included in the trial:
  • Active or past smokers or vapers with less than 1 year since quitting or \>10 pack-year smoking history
  • Unable to tolerate inhalation of gas mixture

Who the study is looking for

  • Subjects must be ≥18 years of age
  • Non-smokers (\<10 pack/year history and no active smoking in the past year)
  • Diagnosis of cystic fibrosis via standard sweat chloride/phenotypic features/genotyping
  • No use of supplemental oxygen
  • Stable lung function (within 10% of personal best in the last 6 months) with no pulmonary exacerbations in the past 4 weeks and baseline FEV1≥60% of predicted
  • Evidence of a personally signed and dated consent indicating that the subject has been informed of all pertinent aspects of the trial
  • Subjects must be willing and able to comply with scheduled visits and other trial procedures

Age in the registry: 18 years to 99 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Univeristy of North Carolina at Chapel Hill
Coordinator of this site? Confirm its status
Chapel HillUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.