NCT06904937

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

57
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
15

participants targeted

Target at below P25 for all trials

Timeline
Completed

Started Jan 2024

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

January 5, 2024

Completed
6 months until next milestone

First Submitted

Initial submission to the registry

July 5, 2024

Completed
9 months until next milestone

First Posted

Study publicly available on registry

April 1, 2025

Completed
8 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2025

Completed
4 days until next milestone

Study Completion

Last participant's last visit for all outcomes

December 5, 2025

Completed
Last Updated

April 1, 2025

Status Verified

July 1, 2024

Enrollment Period

1.9 years

First QC Date

July 5, 2024

Last Update Submit

March 24, 2025

Conditions

Keywords

Inflammatory MyopathyIdiopathic Inflammatory MyopathyRenal biopsy,Guided kidney aspiration biopsy

Outcome Measures

Primary Outcomes (1)

  • Describe the characteristics of patients with inflammatory myopathies

    Up to 1 year

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

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

RECRUITING

MeSH Terms

Conditions

Myositis

Condition Hierarchy (Ancestors)

Muscular DiseasesMusculoskeletal DiseasesNeuromuscular DiseasesNervous System Diseases

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

Locations