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NCT Number: NCT07192679

MAGNIFY - Pulmonary Magnetic Resonance Imaging for Cystic Fibrosis

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.

Recruiting

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Key information

Age range

1 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

University of Sheffield MRI Unit

Sheffield, United Kingdom

Location status: Recruiting

Location contact

Demi-Jade Jakymelen

CONTACT

[email protected]

01142159595

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

General Inclusion criteria

For eligibility into MAGNIFY, subjects should meet all of the following criteria:

  • A confirmed clinical diagnosis of CF, consisting of 2 confirmed disease-causing CFTR mutations along with either positive sweat chloride (>60mmol/L, measured before starting CFTR modulator therapy) or a clinical picture consistent with CF as judged by a senior CF physician. Patients will be under one of named regional CF centres above.
  • Be able to attend the local facility for scans (Royal Hallamshire Hospital, Sheffield).

For eligibility into 129Xe-MRI and lung function (cohort 1,2 and 3)

  • Aged 5 years and above
  • FEV1 >30% predicted (best in the previous 6 months) For eligibility for cohort 1
  • Previous participation in the MMAVIC study, with at least one prior visit where lung ventilation MRI was successfully measured.

For eligibility into cohort 4 for 1H MRI only:

  • Aged between 1 and 5 years of age

General Exclusion criteria

Patients who meet any of the following criteria will be excluded from the study. Further exclusions may be applied at the discretion of the principal investigators.

  • Previous lung transplant.
  • Infection with organisms of the Burkholderia cepacia complex, MRSA or Mycobacterium abscessus.
  • Pregnancy.
  • Resting SpO2 < 90% in room air.
  • Inability to comfortably lie supine for more than 60 minutes.
  • Any contraindication(s) to MRI scanning as per the MRI questionnaire used in clinical practice by the University of Sheffield MRI unit, Royal Hallamshire Hospital.

Research visit (temporary) exclusion criteria

  • Pulmonary exacerbation within 4 weeks as defined by no new treatments in that time, no clinically significant change in their symptoms or spirometry (as judged by attending physician).
  • Pregnancy. Patients who become pregnant prior to consent or during the study can remain in the study. However, no research visits will take place during pregnancy.

Treatment and study plan

Primary outcomes

  1. Ventilation defect percent (VDP) as measured by 129Xe-MRI

    Time frame: Up to 3 years, depending on cohort.

    The primary endpoint will be changes in the 129Xe-MRI metric; ventilation defect percent (VDP) between study visits.

Secondary outcomes

  1. XeMRI outcome measures - Ventilation Heterogeneity Index

    Time frame: up to 3 years

    Similar analysis to the primary outcome will be conducted for Ventilation Heterogeneity Index (VHI)

  2. XeMRI outcome measures - individual defects

    Time frame: up to 3 years

    Similar analysis to the primary outcome will be conducted for the number and size (single measure) of individual defects

  3. XeMRI outcome measures - reversibility index

    Time frame: up to 3 years

    Similar analysis to the primary outcome will be conducted for reversibility index.

  4. Lung function metrics - LCI

    Time frame: Up to 3 years

    Similar analysis will be conducted for the major lung function test metric - LCI, Scond, Sacin (from MBW).

    R5, R5-R20, X5 and Ax from AOS. RV/TLC from body plethysmography. FEV1, FEV1/FVC from spirometry.

  5. Lung function metrics - Scond (from MBW).

    Time frame: Up to 3 years

    Similar analysis will be conducted for the major lung function test metric - Scond, an outcome marker measured from MBW that represents ventilation heterogeneity in the conducting airways within the lung.

    R5, R5-R20, X5 and Ax from AOS. RV/TLC from body plethysmography. FEV1, FEV1/FVC from spirometry.

  6. Lung function metrics - Sacin (from MBW).

    Time frame: Up to 3 years

    Similar analysis will be conducted for the major lung function test metric - Sacin, an outcome marker measured from MBW that represents ventilation heterogeneity in the acinar airways within the lung.

    R5, R5-R20, X5 and Ax from AOS. RV/TLC from body plethysmography. FEV1, FEV1/FVC from spirometry.

Study contacts

Contact information is provided by the study sponsor or research team.

Jim Wild, Professor

CONTACT

[email protected]

01142159595

Sponsors and collaborators

Lead sponsor

Sheffield Teaching Hospitals NHS Foundation Trust

Other

Collaborators

  • University of Sheffield

Registry information

Acronym: MAGNIFY

Important dates

Study start
2024
Primary completion
2029
Study completion
2029
First posted
Sep 25, 2025
Registry last updated
Apr 29, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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