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Cystic Fibrosis (CF)MAGNIFYNCT07192679

MAGNIFY - Pulmonary Magnetic Resonance Imaging for Cystic Fibrosis

An observational study of Cystic Fibrosis (CF), run by Sheffield Teaching Hospitals NHS Foundation Trust at 1 site in United Kingdom.

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Trial summary

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… Read more about this study

Who is it for?
Ages 1 year and older
Conditions the study is for
Cystic Fibrosis (CF)
How many people
60 participants
Where
1 siteUnited Kingdom
Study dates
21 Feb 2024to 30 Jun 2029
Phase
Observational

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 1 year and older
  • All sexes
  • No healthy volunteers
  • Child, Adult, Older adult

Study population: Adults and children with cystic fibrosis

General Inclusion criteria

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

  1. 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.
  2. 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)

  1. Aged 5 years and above
  2. FEV1 >30% predicted (best in the previous 6 months) For eligibility for cohort 1
  3. 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:

  1. 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.

  1. Previous lung transplant.
  2. Infection with organisms of the Burkholderia cepacia complex, MRSA or Mycobacterium abscessus.
  3. Pregnancy.
  4. Resting SpO2 < 90% in room air.
  5. Inability to comfortably lie supine for more than 60 minutes.
  6. 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

  1. 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).
  2. 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.

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Jim Wild, Professor contact

01142159595

sth.magnifystudy@nhs.net

United Kingdom1 site, 1 recruiting
  • University of Sheffield MRI Unit

    Sheffield

    Demi-Jade Jakymelen, 01142159595, sth.magnifystudy@nhs.net

    Recruiting

Other trials in United Kingdom

About this study

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.

Medical subject headings
Cystic Fibrosis

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

Study groups in NCT07192679
Study groupRoleWhat they receive
Cohort 1 - MMAVIC protocolTwenty patients who previously participated in the MMAVIC study, eligible to be on the new regime of CF therapies. These patients will be recruited and invited to attend 4 visits over 3 years.
Cohort 2: Patients not eligible for HEMTA combination of approximately ten children and ten adults who are either not eligible to take HEMT or have not tolerated highly effective modulator treatment (HEMT). Previous MMAVIC participants not on HEMT are also eligible for this cohort. These patients will be invited to attend 3 visits over 2 years.
Cohort 3: School-age children on standard of care treatmentTwenty children who are receiving the current standard of care treatment, including HEMT or other CFTR modulators. These patients will be invited to attend 2 visits - 1 year apart.
Cohort 4: Pre-school children on standard of care treatmentUp to 20 children under the age of 5 years, who are receiving the current standard of care, including CFTR modulator therapies. These participants will have a single visit.
Cohort 5 - MRI repeatabilityAdult participants will be recruited to have repeat MRI scans at various field strengths at 3 sites to assess repeatability of measures.

What is being measured

The primary outcome is the main question the study is designed to answer.

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

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

    Measured: Up to 3 years, depending on cohort.

Secondary outcomes (6)
  1. XeMRI outcome measures - Ventilation Heterogeneity Index

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

    Measured: up to 3 years

  2. XeMRI outcome measures - individual defects

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

    Measured: up to 3 years

  3. XeMRI outcome measures - reversibility index

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

    Measured: up to 3 years

  4. Lung function metrics - LCI

    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.

    Measured: Up to 3 years

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

    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.

    Measured: Up to 3 years

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

    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.

    Measured: Up to 3 years

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted25 Sep 2025
  2. Study start21 Feb 2024
  3. Primary completion30 Jun 2029 (estimated)
  4. Study completion30 Jun 2029 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Other
Time perspective
Prospective
Enrolment
60 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07192679
Sponsor's protocol ID
STH22784
Acronym
MAGNIFY
Status last verified
Apr 2026
First submitted
4 Sep 2025
Last updated
29 Apr 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

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