Actively Recruiting

Phase Not Applicable
Age: 40Years - 85Years
All Genders
Healthy Volunteers
NCT06083467

CW2IP2: Imaging and Diagnostic Assessments

Led by University of Pennsylvania · Updated on 2026-01-07

94

Participants Needed

1

Research Sites

262 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This current protocol will provide the key data to help determine the specificity of our to-be-developed radiotracers by implementing a multi-site diagnostic assessment core and PET imaging of A-beta amyloid (may be completed at some sites as part of another protocol) that is commonly deposited in the brains of people with Parkinson's Disease (PD), Multiple System Atrophy (MSA), Progressive Supranuclear Palsy (PSP) or Frontotemporal Dementia (FTD) as well as healthy controls. This multicenter U19 grant is centered at U Pennsylvania (U Penn) (PI: Robert Mach) in collaboration with U Pittsburgh (Pitt), Yale University, U of California at San Francisco (UCSF) and Washington University in St. Louis (WU). U Penn will act as the single IRB of Record (sIRB) for this multi-center project and subjects will be recruited from all sites.

CONDITIONS

Official Title

CW2IP2: Imaging and Diagnostic Assessments

Who Can Participate

Age: 40Years - 85Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Participants aged 40 to 85 years, both male and female
  • Willing and able to provide written informed consent or have a Legally Authorized Representative (LAR) provide consent
  • Clinical diagnosis confirmed by consensus committee for Parkinson's Disease, Multiple System Atrophy, Progressive Supranuclear Palsy, Frontotemporal Dementia, or healthy control
Not Eligible

You will not qualify if you...

  • Females who are pregnant or breastfeeding at the time of screening
  • Parkinsonism forms other than Parkinson's Disease, Progressive Supranuclear Palsy, and Multiple System Atrophy
  • Major psychiatric disorders such as schizophrenia or bipolar disorder
  • History of significant or ongoing alcohol or substance abuse
  • Contraindications or inability to tolerate imaging, arterial line or IV placement, or blood draw procedures
  • Implanted medical devices or other contraindications to MRI
  • Any current medical condition that could compromise safety or study participation
  • Refusal to consent to postmortem brain donation (except healthy controls)

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

University of Pennsylvania

Philadelphia, Pennsylvania, United States, 19104

Actively Recruiting

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Research Team

E

Erin o Schubert

CONTACT

R

Refatun Momo

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

DIAGNOSTIC

Number of Arms

1

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