Skip to content

Adult Idiopathic Inflammatory Myopathy With Cardiac Injury

A Prospective Cohort Study to Identify a Stratified Approach in the Diagnosis, Treatment in Adult Idiopathic Inflammatory Myopathy With Cardiac Injury

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05982041
Enrollment
300
Registered
2023-08-08
Start date
2024-01-01
Completion date
2043-01-01
Last updated
2023-10-17

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

Conditions

Cardiac Disease, Inflammatory Myopathy

Brief summary

Adult patients with suspected or confirmed idiopathic inflammatory myopathy (IIM) will be recruited. Patients will be approached, consented, have baseline demographics, diagnostics and disease activity measures recorded, and blood taken. The collection of data and biological material will mirror usual clinical practice as far as possible. Subjects will ideally attend further visits at 3, 6 and 12 months to have bloods taken, outcome measures recorded and questionnaires completed.In addition, blood, muscle biopsies and imaging undertaken as part of usual care will also be collected for research purposes to measure a number of biomarkers for the assessment of diagnostic accuracy and clinical utility evaluation. As per usual practice, a muscle biopsy will be performed at baseline, and a further biopsy offered at 6 months to assess treatment response. A magnetic resonance (MR) muscle protocol will also be performed as per usual clinical practice, and a gadolinium-enhanced MR heart scan offered. Both these scans will be repeated at 6-12 months. An existing electronic database entry system will be used for data entry and capture on an anonymised basis.

Interventions

None listed

Sponsors

The First Affiliated Hospital with Nanjing Medical University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

* All patients who had a confirmed (muscular biopsy, electromyogram, magnetic resonance imaging) or suspected clinically myositis * Age over 18 years old * Signature of the informed consent form for the study

Exclusion criteria

* Patients with disease duration \>2 years * Patients \< 18 years * Confirmed non-inflammatory myopathies * Myositis secondary to alcohol or drug abuse * Patients unwilling or unable to give consent * Patients with poor or no venous access

Design outcomes

Primary

MeasureTime frameDescription
The emergence of late gadolinium enhancement (LGE) positive in the different myositis subgroups based on radiological evaluations20 yearsOn the basis of the late gadolinium enhancement (LGE) positive by CMR
The emergence of extra-cellular volume (ECV) > 30% in the different myositis subgroups based on radiological evaluations20 yearsOn the basis of extra-cellular volume (ECV) \> 30% by CMR

Secondary

MeasureTime frameDescription
Number of participants with a significant change levels of diagnostic biomarkers20 yearsThis will depend on the specific biomarker/cytokine being measured
Differences in frequency of genetic variants associated with IIM and subtypes compared to population matched controls20 yearsSpecific identified genetic variants will be identified as part of large scale genetic studies
Incidence of major cardio-vascular events20 years

Contacts

Primary ContactQiang Wang, MD PHD
jerrytortoise@163.com862568307588

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026