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Objective:
To collect information and biospecimens (such as blood, muscle, and skin samples) that will be used to research causes and treatments of inflammatory muscle diseases.
Eligibility:
People aged 12 years and older with suspected or confirmed inflammatory muscle disease. Healthy volunteers aged 18 years and older are also needed.
Design:
Participants will have at least 1 clinic visit. Each visit will last 4 to 8 hours. Some may return for additional visits.
All participants will undergo these procedures (unless they are unable to):
Some procedures are optional:
Full description
Study Description:
This is an observational study to characterize the different types of inflammatory myopathies, understand their etiology, pathogenesis, prognosis, and response to different treatments.
Objectives:
Primary objective: Define the different types of inflammatory muscle diseases, their etiology, pathogenesis, prognostic factors, and response to different treatments.
Secondary objectives: Study different diagnostic modalities that may help to diagnose and monitor the evolution of the disease in patients with myositis.
Endpoints:
Primary endpoint: Severity of muscle, skin, pulmonary, and joint involvement. Study of the immune dysregulation, transcriptomic changes, and genetic modifications in patients with inflammatory muscle diseases.
Secondary endpoints: Utility of standard of care laboratory, radiologic, electrophysiologic, and clinical studies to diagnose and monitor the evolution of the disease in patients with myositis.
Enrollment
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Volunteers
Inclusion and exclusion criteria
In order to be eligible to participate in this study, an individual must meet all of the following criteria:
1. Ability of subject, or Legally Authorized Representative (LAR) to understand and the willingness to sign a written informed consent and/or assent document.
2a. Patients are adults and minors of age 12 or older, with possible inflammatory myopathy (suspected or confirmed)
OR
2b. Healthy volunteers will be adults aged 18 or older.
EXCLUSION CRITERIA:
1. Unwilling to participate in research studies or to provide research samples or data.
500 participants in 2 patient groups
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Central trial contact
Julie G Thompson, R.N.; Andrew L Mammen, M.D.
Data sourced from clinicaltrials.gov
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