Renal Manifestations During Idiopathic Inflammatory Myopathies
IIM
1 other identifier
observational
15
1 country
1
Brief Summary
There are currently no recommendations regarding treatments for Idiopathic Inflammatory Myopathies (IIM) due to the difficulty in conducting high-powered randomized controlled trials. Generally speaking, corticosteroids constitute one of the cornerstones of treatment and are, with some exceptions, always used at least in the initial phase of the disease. In general, this involves oral corticosteroid therapy initiated between 0.5 and 1.5 mg/kg/day followed by a gradual decrease after 4 to 6 weeks of treatment. It is generally necessary to introduce immunosuppressive treatment early with the aim of avoiding corticosteroids. The most commonly used as first-line treatment and having shown effectiveness in observational studies are methotrexate, azathioprine, mycophenolate mofetil and calcineurin inhibitors. In general, rituximab is reserved for severe forms refractory to several first-line immunosuppressants, and has shown some effectiveness during a randomized study. Likewise, cyclophosphamide is only considered in the most severe forms, generally rapidly progressive interstitial lung damage. More recently, Janus kinase inhibitors have been evaluated in several open-label and small-number studies, showing interesting effectiveness, particularly for refractory forms, as shown in this recent review of the literature. Immunoglobulins are the only treatment that has shown superiority compared to placebo in good quality randomized controlled studies. However, due to their cost and difficulty of access, they should be reserved for the severe form, particularly in cases of dysphagia, or refractory form. Apart from these medicinal treatments, it is necessary to add all the non-drug measures which are an integral part of the management of IIM. Performing regular physical activity helps prevent muscle loss and also has a beneficial effect on other comorbidities often present in patients and aggravated by corticosteroid therapy, such as cardiovascular risk factors, osteoporosis and resistance to 'insulin.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for all trials
Started Jan 2024
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 5, 2024
CompletedFirst Submitted
Initial submission to the registry
July 5, 2024
CompletedFirst Posted
Study publicly available on registry
April 1, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 1, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
December 5, 2025
CompletedApril 1, 2025
July 1, 2024
1.9 years
July 5, 2024
March 24, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Describe the characteristics of patients with inflammatory myopathies
Up to 1 year
Eligibility Criteria
Major subject (≥ 18 years old) having inflammatory myopathy and hospitalized at the Strasbourg University Hospital during the period from January 1, 1990 to May 1, 2023.
You may qualify if:
- Major subject (≥ 18 years old)
- Inflammatory myopathy defined by the ACR/EULAR 2017 criteria
- Kidney biopsy performed
- Supported at the Strasbourg University Hospital during the period from January 1, 1990 to May 1, 2023.
- Subject who has not expressed opposition to the reuse of their data for scientific research purposes.
- It is the responsibility of the investigator to verify the absence of opposition in the patient's medical file.
You may not qualify if:
- Subject having expressed opposition to participating in the study
- Known etiology of renal damage excluding inflammatory myopathy.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Service de Rhumatologie - CHU de Strasbourg - France
Strasbourg, 67091, France
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- RETROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
July 5, 2024
First Posted
April 1, 2025
Study Start
January 5, 2024
Primary Completion
December 1, 2025
Study Completion
December 5, 2025
Last Updated
April 1, 2025
Record last verified: 2024-07