Clin2
NCT07454681Possibly a fitNot yet recruiting

MRI scans to check airway changes in cystic fibrosis

Cystic Fibrosis (CF)

Part of Digestive system, Genetic & congenital, Lungs & breathing clinical trials.

This study uses MRI scans to look at the airways in the lungs of children and teens with cystic fibrosis. It aims to see if MRI can detect changes in airway structure, which might help monitor the disease.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Enrollment
76 people
Ages
6 years to 18 years
Study type
Observational

Who can take part

  • You must be between 6 and 18 years old.
  • You must have a diagnosis of cystic fibrosis.
  • You must be able to do a breathing test (spirometry).
  • You cannot have taken oral antibiotics in the past 3 weeks.
  • You cannot have taken new oral or inhaled antibiotics in the past 3 weeks, or IV antibiotics in the past 2 weeks.
  • You cannot need supplemental oxygen or have had a lung or other organ transplant.

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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