Imaging Studies in Corticobasal Syndrome

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorJennifer Whitwell

About this trial

The primary goal of this study is to investigate inflammation and white matter damage in corticobasal syndrome and determine whether these processes are related to each other. The investigator's will address our goal by using neuroimaging and blood plasma biomarkers, as well as molecular pathology.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Age 18 years or older

Meet possible or probable CBS criteria

Disqualifiers

Subjects will be excluded if MRI is contraindicated (due to implanted device, severe claustrophobia, etc)

Subjects will be excluded if they have a concurrent illnesses or structural abnormality that could account for the CBS syndrome

Subjects will be excluded if they have a mutation in the progranulin gene

Subjects will excluded if they have received anti-Aβ therapy

Trial population

All patients who meet criteria are eligible to participate

Trial design

Design model

Case-control

Time perspective

Prospective

Treatments tested in this trial

  • C-11 ER176 Radiotracer

    Diagnostic test

    PET scan looking for inflammation

  • C-11 PiB

    Diagnostic test

    PET scan looking for amyloid protein

  • AV1451 Tau

    Diagnostic test

    Pet scan looking for Tau protein

Treatment groups

80 Participants
are divided into 2 treatment groups
Group A: Corticobasal Syndrome3 interventions
Group B: Healthy Control3 interventions

Trial outcomes

Primary outcomes

1

The investigators will use C-11 ER176 PET imaging to evaluate neuroinflammation and white matter integrity in CBS

Measure whether regional patterns of ER176-PET uptake and white matter microstructure abnormalities using NODDI differ between CBS-4R, CBS-AD, Amn-AD, and HC.

Time frame
approximately 4-5 years into study visits

Secondary outcomes

1

the investigators will use blood samples to assess inflammatory and tau blood plasma metrics in CBS.

Measure whether plasma metrics differ between CBS-4R, CBS-AD, Amn-AD, and HC.

Time frame
approximately 4-5 years into study visits

Other outcomes

1

The investigators will use MR imaging to compare regional markers of inflammation, white matter integrity and tau burden in autopsy tissue from patients with CBS from two different 4R tauopathies and CBS-AD.

Time frame
Approximately 8-10 years after study completion

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Jennifer Whitwell

Lead sponsor

Mayo Clinic

Sponsor institution

National Institute on Aging (NIA)

Collaborator