Parkinson's gene mutation may raise cancer risk – large study investigates
NCT ID NCT06814431
First seen Jul 24, 2026 · Last updated Jul 24, 2026
Summary
This large observational study is investigating whether people with Parkinson's disease who carry a mutation in the GBA1 gene have a higher chance of developing cancer. Researchers will compare cancer rates in this group to those in Parkinson's patients without the mutation and to the general population. The goal is to understand if the GBA1 mutation, already linked to Gaucher disease, also increases cancer risk in Parkinson's patients.
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 a link is found, it could lead to better cancer screening and more comprehensive care for Parkinson's patients with this genetic mutation.
- What could go wrong
- This is an observational study, so it can show an association but not prove cause and effect. The results may not apply to all populations.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 3,000 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Nov 2023
- Expected to finish
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Dec 2026
An estimate. End dates often move.
- Lead sponsor
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A government agency
The lead sponsor is a government body.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Participants will be selected from a network of Italian neurology centers with extensive experience in studying GBA-associated PD, in collaboration with local cancer registries. The study will include approximately 3,000 consecutive PD patients, subdivided into 500 patients with GBA mutations and 2,500 patients with idiopathic PD. These participants will be compared with data from cancer registries to investigate potential associations between GBA mutations and malignancies. The population is drawn from specialized movement disorder centers and represents a clinically well-characterized cohort with access to standardized diagnostic and follow-up procedures.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * \>18 years * Diagnosis of Parkinson's Disease through the United Kingdom Parkinson's Disease Society Brain Bank Diagnostic Criteria for Parkinson's Disease. Exclusion Criteria: * Uncertain diagnosis
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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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
4 sites. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Azienda USL IRCCS di Reggio Emilia
RECRUITINGReggio Emilia, 42123, Italy
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IRCCS Istituto Neurologico Carlo Besta
RECRUITINGMilan, Italy
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Ospedale A. Perrino
RECRUITINGBrindisi, Italy
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Ospedale Santa Chiara di Trento
RECRUITINGTrento, Italy