Scientists hunt for fingerprints of a genetic form of Parkinson's

NCT ID NCT07681219

First seen Jul 02, 2026 · Last updated Jul 02, 2026

Summary

This study aims to find unique biological and clinical markers for a specific genetic form of Parkinson's disease linked to the LRRK2 gene. Researchers will compare 10 people with LRRK2-related Parkinson's to 10 people with sporadic Parkinson's using blood tests, brain MRI scans, and high-density EEG. The goal is to better understand how this form of the disease differs, which could improve diagnosis and guide future 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 could help doctors identify and track LRRK2-related Parkinson's disease more precisely, potentially leading to earlier diagnosis or targeted treatments.

What could go wrong

This is a small, early-stage study with only 20 participants, so findings may not apply to all people with Parkinson's. It is designed to gather information, not to test a treatment.

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.

Parkinson disease

As listed by the trial registrant

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

More trials for these conditions

Other studies related to the condition(s) this trial covers.

Contacts and locations

Study contacts

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