Propranolol in Primary Progressive Aphasia

Part of paid clinical trials in Columbia, Missouri.

Sponsor
University of Missouri-Columbia
Study ID
NCT06066710
Phase
EARLY_PHASE1
Status
Recruiting

Conditions

  • Aphasia, Primary Progressive

Eligibility Criteria

Sex
ALL
Age
50 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • Propranolol — DRUG
    Propranolol will be given on a titration schedule in which participants will begin with small doses of the drug and increase to a larger dosage over the course of three weeks. Propranolol will be taken for a total of 9 weeks.
  • Magnetic Resonance Imaging (MRI) — DEVICE
    Magnetic Resonance Imaging (MRI) will be performed at 3 Tesla and 7 Tesla, for both propranolol and placebo arms.
  • Placebo — DRUG
    Placebo will be given on the same schedule as the propranolol regime.

Study Details

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.

Key Dates

Start date
Jan 13, 2025
Status verified
Mar 2025
Primary completion
Dec 31, 2026
Completion
Dec 31, 2027

Study Design

Enrollment
30 participants (estimated)
Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT

Arms

  • Experimental: Propanolol and MRI
    Participants will receive propranolol via oral capsule. The drug dosage will be titrated slowly to ensure the drug is tolerated well.
  • Placebo Comparator: Placebo and MRI
    Participants will receive placebo via oral capsule.

Primary Outcome Measure

Change in Neuropsychological Assessment Battery Naming Test [ Time Frame: Day 1, 4 Weeks, 8 Weeks, 10 Weeks, 14 Weeks,18 Weeks ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
University of Missouri-ColumbiaColumbiaMissouri65212
David Beversdorf, MD
573-882-6081
Jessica Call
573-882-0515

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