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Characterization of the Serotonin 2A Receptor Selective PET Tracer [18F]MH.MZ in Patients With Neurodegenerative Diseases

Description

It is hypothesize that patients with clinically diagnosed neurodegenerative diseases will have significantly different receptor occupancy of 5HT2A receptors compared to a healthy age/sex-matched control group. This will be tested by measuring 5HT2A receptor density using the PET radioligand (R)-\[18F\]MH.MZ in both populations.

Conditions

Neurodegenerative DiseasesParkinson DiseaseParkinson Disease Psychosis
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Related Conditions:

Neurodegenerative DiseasesParkinson DiseaseParkinson Disease Psychosis

Study Overview

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Study Details

Study overview

It is hypothesize that patients with clinically diagnosed neurodegenerative diseases will have significantly different receptor occupancy of 5HT2A receptors compared to a healthy age/sex-matched control group. This will be tested by measuring 5HT2A receptor density using the PET radioligand (R)-\[18F\]MH.MZ in both populations.

Characterization of the Serotonin 2A Receptor Selective PET Tracer [18F]MH.MZ in Patients With Neurodegenerative Diseases

Characterization of the Serotonin 2A Receptor Selective PET Tracer [18F]MH.MZ in Patients With Neurodegenerative Diseases

Condition
Neurodegenerative Diseases
Intervention / Treatment

-

Contacts and Locations

Nashville

Vanderbilt University Medical Center, Nashville, Tennessee, United States, 37212

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • * Patient arm - clinical diagnosis of Parkinson disease, diffuse Lewy body disease, multiple systems atrophy, Huntington's Disease, Frontotemporal Dementia, and other variants
  • * Healthy arm - age and gender matched to patient arm
  • * Psychosis (presence of hallucinations or delusions) starting after the diagnosis of Parkinson's disease, occurring at least weekly for 4 weeks, severe enough to warrant treatment.
  • * Study partner available for study visits
  • * Prior stroke or other uncontrolled serious neurological or medical illness
  • * Contra-indication or inability to tolerate MRI scan
  • * Use of serotonergic medications in the last 6 weeks
  • * Incapable of providing independent consent.
  • * Pregnant or breastfeeding women
  • * psychosis due to a metabolic, toxic, or primary psychiatric disease
  • * Deemed unable to complete neurocognitive testing
  • * For PD Participants: current or prior use of pimavanserin
  • * Use of antipsychotics in the last 2 weeks

Ages Eligible for Study

50 Years to 85 Years

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

Yes

Collaborators and Investigators

Vanderbilt University Medical Center,

Daniel Claassen, MD, PRINCIPAL_INVESTIGATOR, Vanderbilt University Medical Center

Ciaran Considine, PhD, PRINCIPAL_INVESTIGATOR, Vanderbilt University Medical Center

Richard Darby, MD, PRINCIPAL_INVESTIGATOR, Vanderbilt University Medical Center

Study Record Dates

2025-08