Status:

COMPLETED

Tau Imaging in Young Onset Dementia

Lead Sponsor:

University of Pennsylvania

Conditions:

Alzheimer's Disease, Early Onset

Logopenic Progressive Aphasia

Eligibility:

All Genders

45-70 years

Brief Summary

The central goal of this study is to determine and compare the similarities and differences in regional brain uptake of \[18F\]T807 in patients with typical Alzheimer's Disease (AD), Posterior Cortica...

Eligibility Criteria

Inclusion

  • Participants will be 45 - 70 years of age
  • MMSE \> 10 at screening visit.
  • Participants must be informed of the investigational nature of this study and provide written informed consent in accordance with institutional and federal guidelines prior to study-specific procedures. If the patient is unable to provide informed consent, the patient's legal representative may consent on behalf of the patient but the patient will be asked to confirm assent.
  • Participants must be willing and able to comply with scheduled visits and imaging procedures.
  • A brain MRI is required. If a brain MRI has been performed within 6 months of enrollment to this study and of adequate quality that scan may be used for the study analysis, subjects who do not have a brain MRI will undergo a brain MRI either as a part of this study
  • Participants must identify a study partner who is willing to accompany the patient to study visits

Exclusion

  • Females who are pregnant or breast feeding at the time of screening scan will not be eligible for this study, urine or serum pregnancy test will be performed in women of child-bearing potential at the time of screening
  • Inability to tolerate or contraindication to imaging procedures (PET/CT or MRI) in the opinion of an investigator or treating physician
  • QTc \> 450 msec on screening ECG.
  • Any medical or psychological conditions that, in the opinion of the investigator, would compromise the subject's safety or successful participation in the study (e.g. moderate to large stroke or history of moderate or severe traumatic brain injury (TBI)).

Key Trial Info

Start Date :

November 1 2014

Trial Type :

OBSERVATIONAL

Allocation :

ACTUAL

End Date :

January 31 2019

Estimated Enrollment :

16 Patients enrolled

Trial Details

Trial ID

NCT02289118

Start Date

November 1 2014

End Date

January 31 2019

Last Update

March 25 2020

Active Locations (1)

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1

University of Pennsylvania

Philadelphia, Pennsylvania, United States, 19104