Scientists hunt for genetic clues to rare bone and skin disease
NCT ID NCT07081880
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study aims to uncover the genetic and immune factors behind SAPHO syndrome, a rare chronic condition causing bone inflammation and skin issues. Researchers will collect DNA and cells from 100 adults diagnosed with SAPHO to compare their genetic makeup with the general population. The goal is to better understand what causes the disease and why it varies so much between patients, which could eventually lead to more accurate diagnosis and tailored treatments.
What this could mean
Our plain-language read of the trial. This is informational only — not medical advice or a prediction.
- What this could lead to
- If successful, this research could uncover genetic markers that help diagnose SAPHO syndrome more accurately and point toward more personalized treatments.
- What could go wrong
- This is an observational study, not a treatment trial. It may not lead directly to new therapies, and results may take years to translate into clinical practice.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Hôpital Cochin
RECRUITINGParis, France
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Hôpital Paris Saint Joseph
RECRUITINGParis, France
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Other studies related to the condition(s) this trial covers.