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DEtection of Cellular Inflammation With FERumoxytol in the HEART

DEtection of Cellular Inflammation With FERumoxytol in the HEART

Status
Completed
Phases
Phase 2Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02319278
Acronym
DECIFER
Enrollment
58
Registered
2014-12-18
Start date
2014-12-31
Completion date
2016-11-30
Last updated
2017-05-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cardiac Sarcoid, Cardiac Transplant, Healthy Volunteers, Myocarditis

Brief summary

To non-invasively image myocardial accumulation of ultrasmall superparamagnetic particles of iron oxide (USPIOs) by an increase in R2\* values (compared to controls) within the myocardium of patients with: i. cardiac transplantation ii. acute myocarditis iii. suspected cardiac sarcoidosis

Detailed description

Ferumoxytol is a 'smart' magnetic resonance contrast agent consisting of ultrasmall superparamagnetic particles of iron oxide (USPIOs) that are taken up by macrophages. Concentration of USPIOs within macrophages changes the tissue relaxation properties and this can be detected by magnetic resonance imaging using R2\* maps. In a recent early proof-of-concept study, we demonstrated that macrophages could be detected with USPIOs in the penumbra and infarct zone of the myocardium in patients with a recent myocardial infarction. The investigators therefore wish to establish whether USPIOs can be used to identify cellular inflammation within the myocardium in three distinct clinical conditions that currently lack a non-invasive diagnostic imaging test: cardiac allograft rejection, viral myocarditis and cardiac sarcoidosis. If successful, this would not only provide a useful diagnostic test but would also be a method of monitoring disease progression or response to therapy.

Interventions

DRUGFerumoxytol

Infusion following between paired MRI scans

Sponsors

Royal Infirmary of Edinburgh
CollaboratorOTHER
Golden Jubilee National Hospital
CollaboratorOTHER_GOV
Royal Brompton & Harefield NHS Foundation Trust
CollaboratorOTHER
University of Edinburgh
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

1. One of the four conditions below: * Patients having undergone cardiac transplant * Patients diagnosed clinically with myocarditis of any aetiology (eg viral, septic, post chemotherapeutic etc) * Patients clinically diagnosed with cardiac sarcoidosis * Healthy volunteers 2. Age \> 18 years.

Exclusion criteria

1. Contraindication to magnetic resonance imaging scanning identified from magnetic resonance imaging safety questionnaire 2. Patients refusing or unable to give informed consent 3. Renal failure (estimated glomerular filtration rate \<30 mL/min) 4. Polycythemia 5. Contraindication to ferumoxytol (previous allergic drug reaction, any immune or inflammatory conditions (eg, systemic lupus erythematosus, rheumatoid arthritis, history of severe asthma, eczema or other atopic allergy)), evidence of known iron overload, hemochromatosis, known hypersensitivity to ferumoxytol or its components or anaemia not caused by iron deficiency. 6. Known allergy to dextran- or iron-containing compounds. 7. Diagnosis of myocardial infarction within 1 month. 8. Pregnancy or Breast-feeding. 9. Women of child bearing age not ensuring reliable methods of contraception. Female participants of child bearing age will be asked if they are ensuring reliable methods of contraception prior to each administration of USPIO and MRI scan. If use of reliable contraception cannot be confirmed, the participant will be withdrawn.

Design outcomes

Primary

MeasureTime frameDescription
Assessment of Myocardial Cellular Inflammation.1 yearAssessment of Myocardial Cellular Inflammation through the increase in R2\* value on post USPIO imaging versus baseline imaging.

Secondary

MeasureTime frameDescription
Correlation of R2* values with circulating inflammatory markers1 yearComparison of circulating inflammatory markers in peripheral blood with myocardial inflammation (seen on cardiac R2\* maps) .
Does clinical condition correlate with inflammation seen on R2* maps. (assessed by reduction in R2* values)1 yearDoes treatment or recovery from these inflammatory myocardial conditions reduce or halt uptake of USPIOs as assessed by reduction in R2\* values.
Do higher R2* correlate with poorer outcome? (assessed by deterioration in ejection fraction or increase in late gadolinium enhancement)1 yearDo patients with higher R2\* values have worse outcomes assessed by deterioration in ejection fraction or increase in late gadolinium enhancement.

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 12, 2026