Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| Name | Class |
|---|---|
| University of Sheffield | OTHER |
Not provided
Not provided
Not provided
Not provided
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.
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| Label | Type | Description | Intervention Names |
|---|---|---|---|
| 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. |
Not provided
| Measure | Description | Time Frame |
|---|---|---|
| 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. | Up to 3 years, depending on cohort. |
| Measure | Description | Time Frame |
|---|---|---|
| XeMRI outcome measures - Ventilation Heterogeneity Index | Similar analysis to the primary outcome will be conducted for Ventilation Heterogeneity Index (VHI) | up to 3 years |
| XeMRI outcome measures - individual defects |
Not provided
General Inclusion criteria
For eligibility into MAGNIFY, subjects should meet all of the following criteria:
For eligibility into 129Xe-MRI and lung function (cohort 1,2 and 3)
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:
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.
Research visit (temporary) exclusion criteria
Not provided
Not provided
Not provided
Adults and children with cystic fibrosis
| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Jim Wild, Professor | Contact | 01142159595 | sth.magnifystudy@nhs.net |
Not provided
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| University of Sheffield MRI Unit | Recruiting | Sheffield | United Kingdom |
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| ID | Term |
|---|---|
| D003550 | Cystic Fibrosis |
| ID | Term |
|---|---|
| D010182 | Pancreatic Diseases |
| D004066 | Digestive System Diseases |
| D008171 | Lung Diseases |
| D012140 | Respiratory Tract Diseases |
Not provided
Not provided
Not provided
Not provided
Not provided
Similar analysis to the primary outcome will be conducted for the number and size (single measure) of individual defects
| up to 3 years |
| XeMRI outcome measures - reversibility index | Similar analysis to the primary outcome will be conducted for reversibility index. | 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. | 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. | 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. | Up to 3 years |
| D030342 |
| Genetic Diseases, Inborn |
| D009358 | Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
| D007232 | Infant, Newborn, Diseases |