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Recruiting NCT07000851

NCT07000851 Imaging Studies in Corticobasal Syndrome

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Clinical Trial Summary
NCT ID NCT07000851
Status Recruiting
Phase
Sponsor Jennifer Whitwell
Condition Cortico Basal Degeneration
Study Type OBSERVATIONAL
Enrollment 80 participants
Start Date 2025-06-25
Primary Completion 2030-03-30

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age N/A
Study Type OBSERVATIONAL
Interventions
C-11 ER176 RadiotracerC-11 PiBAV1451 Tau

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.

This trial targets 80 participants in total. It began in 2025-06-25 with a primary completion date of 2030-03-30.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

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

Inclusion Criteria: * Age 18 years or older * Meet possible or probable CBS criteria Exclusion Criteria: * 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 * Women who are pregnant will be excluded * Subjects will be excluded if they are actively taking daily anti-inflammatory medications (NSAIDs, corticosteriods, etc) * Subjects will be excluded if they have generalized inflammatory condition and treatment with immunosuppressive, corticoid/glucocorticoid, steroidal or non-steroidal anti-inflammatory medication within 2 weeks of scanning

Contact & Investigator

Central Contact

Megan J Meyer, M.B.A.

✉ meyer.megan6@mayo.edu

📞 507-293-1164

Principal Investigator

Jennifer Whitwell, Ph.D.

PRINCIPAL INVESTIGATOR

Mayo Clinic

Frequently Asked Questions

Who can join the NCT07000851 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, studying Cortico Basal Degeneration. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07000851 currently recruiting?

Yes, NCT07000851 is actively recruiting participants. Contact the research team at meyer.megan6@mayo.edu for enrollment information.

Where is the NCT07000851 trial being conducted?

This trial is being conducted at Rochester, United States.

Who is sponsoring the NCT07000851 clinical trial?

NCT07000851 is sponsored by Jennifer Whitwell. The principal investigator is Jennifer Whitwell, Ph.D. at Mayo Clinic. The trial plans to enroll 80 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology