Rare disease study aims to uncover secrets of harmful calcium buildup

NCT ID NCT07285421

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study looks at people with Enamel Renal Syndrome, a rare genetic condition that causes calcium deposits in the body, leading to kidney and blood vessel problems. Researchers will measure kidney function and test how the body handles calcium, phosphate, water, and acid. The goal is to better understand what causes these calcium deposits. The study involves 30 patients and some healthy volunteers for comparison.

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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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Conditions

The condition(s) this trial relates to.

amelogenesis imperfecta type 1G

As listed by the trial registrant

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

Contacts and locations

Study contacts

  • Contact

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

  • Contact

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

Locations

  • HEGP - clinical investigation center

    Paris, 75015, France

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

    Contact

  • HEGP - physiology department

    Paris, 75015, France

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

    Contact