Early Phase 1 Parkinson's Disease Trial, Recruiting NCT06098612 Sponsor: Massachusetts General Hospital Condition: Parkinson's Disease
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Early Phase 1 Parkinson's Disease Trial, Recruiting

NCT06098612
Recruiting Early Phase 1

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • You are between 50 and 80 years old
  • You are able to sign a consent form agreeing to take part
  • You can read, speak, and understand English
  • You are willing and able to take part in one brain scanning session (PET/MRI)

If you have Parkinson's disease (PD), you also need to:

  • Have an existing diagnosis of Parkinson's disease based on standard criteria
  • Have been on stable medications for at least 30 days
  • Have a disease stage between I and IV on a standard Parkinson's rating scale (confirm with trial site)
  • Have a family member or caregiver who can answer questions about your daily activities

If you have Multiple System Atrophy (MSA), you also need to:

  • Have an existing diagnosis of MSA based on standard criteria
  • Have been on stable medications for at least 30 days
  • Have either the movement-focused or balance/coordination-focused type of MSA (confirm with trial site)
  • Have a family member or caregiver who can answer questions about your daily activities

If you have Dementia with Lewy Bodies (DLB), you also need to:

  • Have an existing diagnosis of probable DLB based on standard criteria
  • Have been on stable medications for at least 30 days
  • Have a mild level of cognitive impairment or less, based on a standard memory and thinking scale (confirm with trial site)
  • Have a family member or caregiver who can answer questions about your daily activities

Who may not be able to join:

  • You have risk factors for heart or blood vessel disease (such as high blood pressure or high cholesterol) that are not well managed
  • You have a major psychiatric condition such as schizophrenia
  • You have a history of stroke
  • A previous brain scan has shown specific areas of damage in your brain
  • You have a history of serious illness, including major kidney or liver problems or a significant brain or nerve condition
  • You have had major surgery in the past 6 months
  • You have a history of head injury from an external force, such as a blow to the head, a blast, or a penetrating injury
  • You have problems with urination that are not being treated or managed
  • You have a current or past diagnosis of bipolar disorder or certain other mental health conditions (note: treated depression is allowed)
  • You currently misuse drugs or alcohol
  • You are unable to lie flat and still for up to 90 minutes during the scan
  • You are pregnant or breastfeeding
  • You have metal objects in your body that could be affected by the MRI scanner, or you have a fear of enclosed spaces that would prevent you from having an MRI
  • You have recently been exposed to radiation from other research scans, and combining that with this study would exceed safe limits
  • You have certain metal implants in your body, such as aneurysm clips, artificial heart valves with metal parts, metal fragments, shrapnel, or ferromagnetic (metal-attracting) jewellery or clothing clips
  • You have an electrical implant such as a heart pacemaker or a medication pump
  • You have a medical condition that increases your risk of seizures, severe anxiety in enclosed spaces, or cardiac arrest
  • You are unable to lie comfortably on a flat bed inside the scanner for 60 to 90 minutes due to conditions such as back pain or arthritis
  • You are a woman of childbearing age and do not have a negative pregnancy blood test on the day of the scan
  • You weigh more than 300 lbs (the weight limit for the MRI table)

If your participation involves a blood draw through an arterial line during the scan, you may also not be able to join if:

  • A standard circulation test on both your hands gives an abnormal result (confirm with trial site)
  • You have Raynaud's syndrome (a condition affecting blood flow to the fingers)
  • You have a bleeding disorder
  • You take blood-thinning medications such as Coumadin, Plavix, or Lovenox
  • You have an allergy to Lidocaine (a local anaesthetic)

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 27 July 2026
Early Phase 1 studies are small, early exploratory studies that come before the main Phase 1 to 3 testing, so a standard phase success rate does not apply.

Contact this trial

Phone: 6177243983

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Early Phase 1
Registry
ClinicalTrials.gov
Start date
1 May 2024
Est. completion
1 November 2026

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

brain uptake evaluation

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 27 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov