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Non-invasive Brain Stimulation

MagStim Rapid2 Transcranial Magnetic Simulation for Primary Progressive Aphasia

N/A
Waitlist Available
Led By Michelle Tsang, MD
Research Sponsored by University of Manitoba
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up one week pre- and one week post-rtms treatment
Awards & highlights

Study Summary

This trial will investigate whether rTMS can improve language functioning in people with primary progressive aphasia-logopenic variant.

Eligible Conditions
  • Primary Progressive Aphasia

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~one week pre- and one week post-rtms treatment
This trial's timeline: 3 weeks for screening, Varies for treatment, and one week pre- and one week post-rtms treatment for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Change in score on the Druks and Masterson Naming Task

Trial Design

1Treatment groups
Experimental Treatment
Group I: Repetitive Transcranial Magnetic Stimulation (rTMS)Experimental Treatment1 Intervention
30 sessions of high-frequency (10Hz) repetitive stimulation applied over the posterior region of the left superior temporal gyrus in patients with logopenic primary progressive aphasia (PPA-L) using a MagStim Rapid2 Transcranial Magnetic Simulation machine.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
MagStim Rapid2 Transcranial Magnetic Simulation
2022
N/A
~30

Find a Location

Who is running the clinical trial?

University of ManitobaLead Sponsor
595 Previous Clinical Trials
199,512 Total Patients Enrolled
Mandana Modirrousta, MD PhDStudy DirectorUniversity of Manitoba
2 Previous Clinical Trials
40 Total Patients Enrolled
Michelle Tsang, MDPrincipal InvestigatorUniversity of Manitoba

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
~2 spots leftby Apr 2025