Actively Recruiting

Age: 1Year +
All Genders
NCT07192679

MAGNIFY - Pulmonary Magnetic Resonance Imaging for Cystic Fibrosis

Led by Sheffield Teaching Hospitals NHS Foundation Trust · Updated on 2026-04-29

60

Participants Needed

1

Research Sites

279 weeks

Total Duration

On this page

Sponsors

S

Sheffield Teaching Hospitals NHS Foundation Trust

Lead Sponsor

U

University of Sheffield

Collaborating Sponsor

AI-Summary

What this Trial Is About

This research study is looking at new ways of measuring the function of the lungs in patients with cystic fibrosis. This study is using the most advanced methods for measuring lung function including 2 tests called hyperpolarised gas magnetic resonance imaging (HP MRI) and multiple breath washout (MBW), to better understand changes in the lungs over time. HP MRI involves taking pictures of the air in your lungs after breathing in a harmless gas (xenon). MBW is a breathing test used to calculate something called the lung clearance index (LCI). By measuring these tests on the same day, alongside standard lung function tests, we aim to understand lung function in greater detail than ever before.

CONDITIONS

Official Title

MAGNIFY - Pulmonary Magnetic Resonance Imaging for Cystic Fibrosis

Who Can Participate

Age: 1Year +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Confirmed clinical diagnosis of cystic fibrosis with 2 disease-causing CFTR mutations and positive sweat chloride (>60 mmol/L) or clinical confirmation by a senior CF physician
  • Able to attend the Royal Hallamshire Hospital in Sheffield for scans
  • For 129Xe-MRI and lung function cohorts (1, 2, and 3): aged 5 years or older
  • For cohort 1: FEV1 greater than 30% predicted (best in previous 6 months)
  • Previous participation in the MMAVIC study with at least one prior lung ventilation MRI measurement (for cohort 1)
  • For cohort 4 (1H MRI only): aged between 1 and 5 years
Not Eligible

You will not qualify if you...

  • Previous lung transplant
  • Infection with Burkholderia cepacia complex, MRSA, or Mycobacterium abscessus
  • Pregnancy (except participants who become pregnant after consent; no research visits during pregnancy)
  • Resting oxygen saturation (SpO2) below 90% in room air
  • Unable to lie comfortably on their back for more than 60 minutes
  • Any contraindications to MRI scanning as per hospital MRI questionnaire
  • Pulmonary exacerbation within 4 weeks before research visit (no new treatments or symptom changes during that time)

AI-Screening

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Trial Site Locations

Total: 1 location

1

University of Sheffield MRI Unit

Sheffield, United Kingdom

Actively Recruiting

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Research Team

J

Jim Wild, Professor

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

5

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