AP-HP, Pitié-Salpêtrière Hospital, Department of Internal Medicine and clinical immunology
Paris, 75013, France
NCT Number: NCT04637672
Myositis are rare diseases for which the development of a cohort associated with a bank of biological samples (biobank) will allow for the conduct of researches to better delineate the underlying pathophysiology and find cures. This prospective cohort of patients with myositis will allow for identification of factors favouring the occurrence of myositis, whether they are constitutional (genetic) or acquired (environmental or drug). Different subgroups of myositis used for prognostication will be identified based on clinico-demographical variables, the nature of the organs involved beyond peripheral muscles (cardiac, diaphragm) and biomarkers abnormalities.
Looking for future studies?
Notify Me18 year and older
All sexes
Observational
Paris, 75013, France
Myositis is a rare autoimmune disease in which the immune system mistakenly attacks the patient's own peripheral muscles. This aggression manifests by muscle inflammation and necrosis responsible for a motor deficit of varying severity.
The treatments available today are insufficient and are non-specific. Biological criteria, issued from simple blood or muscle tests are missing, and they will help to define the activity of the disease and the efficacy of treatments.
The MASC protocol will include patients with myositis, and investigators will collect clinical, radiological, electrophysiological, histological and biological data to be used for researches aiming at better understanding this entity. A biobank (muscle biopsy, DNA, serum, plasma, PBMCs) will be acquired on this prospective cohort.
The study itself will be composed of a baseline visit and monthly to yearly follow-up visits which will assess:
Patient activity assessment: evaluation of daily life activity by both patient and physician using a Visual Analogue Scale
For each patient, the date of last visit or contact will be collected as well as outcomes, particularly for the cause of death if relevant.
Data from the biobank MASC " Muscles DNA/RNA Serum and Cells " will be added to other data. The biobank has been fully registered with local authorities and ethical committees ("Committee for Personal Protection (CPP)" CPP agreement). It contains peripheral blood mononuclear cells (PBMC), serum, DNA and RNA from blood and muscular biopsies collected at the diagnosis stage. The database contains immunological and genetical data.
This prospective study will also aim at:
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Time frame: baseline: first 30 days after inclusion
Characterisation of the different myositis subgroups based on clinical, radiological, electrophysiological and histo-biological evaluations, including but not limited to: sexe, age, profession, a history of infection, cancer or other autoimmune and inflammatory diseases, diagnosis criteria, creatine phosphokinase, autoantibodies, immune systeme evaluation based on peripheral blood mononuclear cells, DNA sequencing muscular biopsies
Time frame: up to twenty years after inclusion
Characterisation of the natural history of myositis subgroups :responses to treatments, prognosis factors, evolution
Time frame: baseline: first 30 days after inclusion
Characterisation of an immune system signature, using peripheral blood mononuclear cells and muscular biopsies, DNA and RNA sequencing, and autoantibodies
Time frame: up to twenty years after inclusion
Risk factors for All-cause mortality depending on patient's and disease characteristics including clinical, radiological electrophysiological, histo-biological and immunological as well as treatment received stratified by each subgroup of myositis
Time frame: up to twenty years after inclusion
Change of the quality of life, using quality of life questionnaires, depending of patients and disease characteristics
Time frame: up to twenty years after inclusion
Change of activity impairment using an evaluation of daily life activity by both patient and physician using a Visual Analogue Scale depending of patients and disease characteristics
Time frame: up to twenty years after inclusion
Characterisation of a quality-of-life scale using biological data (CPK), muscle weakness (muscle testing) and other visceral involvements
Time frame: up to twenty years after inclusion
Characterisation of a global activity scale using biological data (CPK), muscle weakness (muscle testing) and other visceral involvements
Time frame: up to twenty years after inclusion
Incidence of major cardio-vascular events
Time frame: up to twenty years after inclusion
Consequences on outcomes of major cardio-vascular events
Time frame: up to twenty years after inclusion
Correlation of myositis with the development of extra-muscular diseases including but not limited to dermatological, rheumatological, cardiological and pneumological associated diseases
Time frame: up to twenty years after inclusion
Characterisation of respiratory function with pulmonary function test and thoracic tomodensitometry
Time frame: up to twenty years after inclusion
Characterisation of diaphragmatic failure with pulmonary function test and thoracic tomodensitometry
Time frame: up to twenty years after inclusion
Follow up of respiratory function with pulmonary function test and thoracic tomodensitometry
Time frame: up to twenty years after inclusion
Follow up of diaphragmatic failure with pulmonary function test and thoracic tomodensitometry
Groupe Hospitalier Pitie-Salpetriere
Other
Acronym: MASC
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT05454527
Drug-induced Inflammatory Myositis, Idiopathic Inflammatory Myositis
Paris, France
View Trial DetailsNCT03757065
Arthritis, Arthritis, Rheumatoid
Vancouver, British Columbia, Canada
View Trial DetailsNCT07301164
ANCA Associated Vasculitis, Anti-Neutrophil Cytoplasmic Antibody-Associated Vasculitis
View Trial DetailsNCT06642870
ANCA Associated Vasculitis (AAV), Anti-Neutrophil Cytoplasmic Antibody-Associated Vasculitis
Bristol, United Kingdom
View Trial Details