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.
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:
- 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.
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
United Kingdom1 site, 1 recruiting
- Recruiting
University of Sheffield MRI Unit
Sheffield
Demi-Jade Jakymelen, 01142159595, sth.magnifystudy@nhs.net
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.
- Conditions
- Cystic Fibrosis (CF)
- 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 group | Role | What they receive |
|---|---|---|
| Cohort 1 - MMAVIC protocol | Twenty 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 HEMT | A 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 treatment | Twenty 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 treatment | Up 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 repeatability | Adult 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.
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)
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
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
XeMRI outcome measures - reversibility index
Similar analysis to the primary outcome will be conducted for reversibility index.
Measured: up to 3 years
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
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
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.
- First posted25 Sep 2025
- Study start21 Feb 2024
- Primary completion30 Jun 2029 (estimated)
- Study completion30 Jun 2029 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Cystic Fibrosis (CF)Studies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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)
Sponsor and investigators
- Lead sponsor
- Sheffield Teaching Hospitals NHS Foundation Trust
- Sponsor type
- University, hospital or other
- Collaborators
- University of Sheffield
- Responsible party
- Sponsor
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