New registry aims to shed light on angelman syndrome

NCT ID NCT03650569

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

Summary

This completed registry study collected information from 82 people with Angelman syndrome in Italy. The goal was to track medical and behavioral problems linked to the condition. No treatments or interventions were tested; instead, the data will help researchers better understand Angelman syndrome and potentially improve future care.

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 registry could help researchers better understand Angelman syndrome and improve care for those affected.

What could go wrong

This is an observational registry, not a treatment trial, so it will not directly lead to new therapies. Results depend on the quality of data provided by participants.

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.

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Conditions

The condition(s) this trial relates to.

Angelman syndrome Rare Diseases

As listed by the trial registrant

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

Contacts and locations

Locations

  • FROM - Research Foundation Bergamo Hospital - ETS, Bergamo, Italy

    Bergamo, 24127, Italy