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Clinical Trial Summary

The purpose of this study is to find out how the language of people with Primary Progressive Aphasia is affected by Propranolol. Propranolol is not FDA approved for the treatment of Primary Progressive Aphasia. Propranolol is FDA approved for the treatment of heart conditions such as blood pressure. This research is being done because there are currently no drug treatment options for language impairments and anxiety often experienced by people with Primary Progressive Aphasia.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06066710
Study type Interventional
Source University of Missouri-Columbia
Contact David Beversdorf, MD
Phone 573-882-6081
Email beversdorfd@health.missouri.edu
Status Recruiting
Phase Early Phase 1
Start date May 2024
Completion date October 2026

See also
  Status Clinical Trial Phase
Active, not recruiting NCT02675270 - Rehabilitation and Prophylaxis of Anomia in Primary Progressive Aphasia N/A
Not yet recruiting NCT05437159 - Investigating Speech Sequencing in Neurotypical Speakers and Persons With Disordered Speech N/A
Withdrawn NCT03448133 - rTMS for the Treatment of Primary Progressive Aphasia: A Randomized Controlled Trial N/A
Active, not recruiting NCT04937452 - Dopaminergic Therapy for Frontotemporal Dementia Patients Phase 2