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New study explores blood, skin, and nasal swabs to spot Parkinson's early

NCT ID NCT07480187

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing This study
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study is looking for better ways to diagnose Parkinson's disease using samples that are easy to collect, like blood, skin, and nasal swabs. Researchers will compare these samples from 340 people, including those with Parkinson's, Alzheimer's, and healthy volunteers. The goal is to find biological markers that could lead to a simpler, more accurate diagnosis.

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 lead to a simple, non-invasive test for Parkinson's disease, enabling earlier diagnosis and better clinical trials.
What could go wrong
This is an observational study, not a treatment trial. The biomarkers may not prove accurate enough for widespread use, and results may not apply to all patients.

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.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

340 people

The number who actually took part.

Started

May 2023

Expected to finish

May 2026

An estimate. End dates often move.

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

30 years and older

Sex

Anyone

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

Show 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: patients with clinical diagnosis of Parkinson's disease, atypical parkinsonisms, Alzheimer's disease, healthy volunteers, people with subjective cognitive decline. Exclusion Criteria: Other acute neurological diseases or neurodegenerative diseases such as Frontotemporal dementia, vascular dementia, and stroke Relevant comorbidities: chronic kidney disease (significant alteration of blood biomarkers) Skin biopsy: local skin infection at biopsy site, severe dermatologic disease at sampling area, known bleeding disorder, significant thrombocytopenia, anticoagulation not safely manageable, allergy to local anesthetics, poor wound healing, severe peripheral vascular disease, high-risk immunosuppression, inability to consent or cooperate, extensive scarring at intended site Magnetic resonance spectroscopy: non-MRI-compatible implanted device, ferromagnetic intracranial clip, metallic foreign body, severe claustrophobia not manageable, inability to remain still, MRI-conditional device not meeting safety conditions, pregnancy per institutional policy, severe agitation or confusion, body size exceeding scanner limits, severe motion disorder affecting acquisition Venipuncture: refusal or inability to consent, local infection at puncture site, severe coagulopathy, marked thrombocytopenia, high bleeding risk anticoagulation, severe anemia relative to planned blood volume, difficult venous access, history of severe vasovagal syncope Eligibility Criteria Inclusion Criteria: Adults able to provide informed consent Clinical diagnosis of Parkinson's disease Clinical diagnosis of atypical parkinsonism Clinical diagnosis of Alzheimer's disease Individuals with subjective cognitive decline Healthy volunteers Exclusion Criteria: Acute neurological diseases Other neurodegenerative diseases not included in the study groups (e.g., frontotemporal dementia, vascular dementia) History of stroke with significant neurological sequelae Chronic kidney disease with significant alteration of blood biomarkers Procedure-specific exclusion criteria Skin biopsy: Local skin infection at biopsy site Severe dermatologic disease at sampling area Known bleeding disorder Significant thrombocytopenia Anticoagulation not safely manageable Allergy to local anesthetics Poor wound healing Severe peripheral vascular disease High-risk immunosuppression Inability to consent or cooperate Extensive scarring at intended biopsy site Magnetic resonance spectroscopy (MRS): Non-MRI-compatible implanted device Ferromagnetic intracranial clip Metallic foreign body incompatible with MRI Severe claustrophobia not manageable with standard procedures Inability to remain still during MRI acquisition MRI-conditional device not meeting safety conditions Pregnancy according to institutional MRI safety policy Severe agitation or confusion preventing examination Body size exceeding scanner limits Severe motion disorder affecting acquisition Venipuncture: Refusal or inability to provide consent Local infection at puncture site Severe coagulopathy Marked thrombocytopenia High bleeding risk due to anticoagulation Severe anemia relative to planned blood draw volume Difficult venous access History of severe vasovagal syncope during venipuncture Lumbar puncture: Signs of increased intracranial pressure due to mass lesion Local infection at puncture site Uncorrected coagulopathy Severe thrombocytopenia Anticoagulation not safely interruptible Spinal cord compression Unstable spine Refusal or inability to cooperate with the procedure Severe spinal deformity Prior lumbar surgery complicating access Severe anxiety or intolerance to the procedure Pregnancy requiring procedural precautions Nasal brushing: Significant nasal polyposis Severe septal deviation preventing access to the olfactory cleft Active acute or chronic rhinosinusitis Recent epistaxis or bleeding-prone nasal mucosa Nasal lesions, ulcers, or tumors Recent nasal surgery Nasal brushing: Significant nasal polyposis, Severe septal deviation preventing access to the olfactory cleft, Active acute or chronic rhinosinusitis, Recent epistaxis or bleeding-prone nasal mucosa, Nasal lesions, ulcers, tumors, or recent nasal surger

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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.

Contacts and locations

Locations

  • Azienda Ospedaliera di Perugia

    Perugia, 06129, Italy

  • Centro Neurolesi Bonino Pulejo

    Messina, Messina, 98124, Italy

  • Istituto Neurologico Carlo Besta

    Milan, Milano, 20133, Italy

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