New eye scan may spot early damage in rare genetic disease

NCT ID NCT07006649

First seen Dec 24, 2025 · Last updated Jun 22, 2026 · Updated 20 times

Summary

This study looks at whether a special eye scan can detect early blood flow changes in the retina of people with pseudoxanthoma elasticum (PXE), a rare genetic disease that can cause vision loss. Researchers will compare 30 PXE patients with 30 healthy volunteers matched by age and gender. The goal is to find a reliable marker to track the disease, not to test a treatment.

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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.

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Contacts and locations

Study contacts

  • Contact

    Phone: •••-•••-•••• Email: •••••@•••••

  • Contact

    Phone: •••-•••-•••• Email: •••••@•••••

Locations

  • Angers University Hospital

    RECRUITING

    Angers, 49000, France

    Contact Phone: •••-•••-•••• Email: •••••@•••••

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 could identify a way to track PXE eye damage earlier, helping future studies measure disease progression.

What could go wrong

This is an early observational study with only 60 people. It does not test any treatment, so it cannot directly improve vision or slow the disease.

Conditions

The condition(s) this trial relates to.

autosomal recessive inherited pseudoxanthoma elasticum pseudoxanthoma elasticum (inherited or acquired) retinal disorder

As listed by the trial registrant

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