Den här översättningen är inte klar ännu. Den här sidan är just nu på engelska.

Gå till den engelska sidan

Early IVIg may boost myositis recovery

NCT ID NCT05832034

First seen Feb 28, 2026 · Last updated Jun 23, 2026 · Updated 13 times

Summary

This study tests whether adding intravenous immunoglobulin (IVIg) to standard steroid treatment early in myositis helps patients improve faster. It includes 44 adults with recent-onset myositis (less than 12 months). Participants receive either IVIg or a placebo alongside steroids, and improvement is measured after 12 weeks.

Disclaimer Read more

This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.

Get updates

Get notified about this study

Sign up to get updates when this study changes or when new studies for DERMATOMYOSITIS are added.

Vår säkerhetsrekommendation!

Genom att skicka in godkänner du våra Användarvillkor

Contacts and locations

Locations

  • Department of Neurology, Amsterdam UMC, location AMC

    Amsterdam, North Holland, 1105 AZ, Netherlands

What this could mean

Our plain-language read of the trial. This is informational only — not medical advice or a prediction.

Active substance

Immune Globulin Intravenous (Human) (IVIg)

What this could lead to

If it works, this could mean a faster, more effective way to control myositis early, potentially preventing long-term disability.

What could go wrong

This is a small, early-phase trial (44 participants). The benefit may be modest, and IVIg can cause side effects like headaches or allergic reactions.

Conditions

The condition(s) this trial relates to.

antisynthetase syndrome dermatomyositis myositis disease polymyositis

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.