Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT04188067 · ClinicalTrials.gov registry record · NA

TMS for the Treatment of Primary Progressive Aphasia

A NA study of Logopenic Variant Primary Progressive Aphasia and Non-fluent Variant Primary Progressive Aphasia, sponsored by Massachusetts General Hospital.

Completed
Registry status
NA
Development phase
10
Enrollment target
1
Study location

NCT04188067 is a NA study of Logopenic Variant Primary Progressive Aphasia and Non-fluent Variant Primary Progressive Aphasia that has completed, run by Massachusetts General Hospital. The registered enrollment target is 10 participants. The trial reports 1 study location across 1 state.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT04188067, a NA study of Logopenic Variant Primary Progressive Aphasia and Non-fluent Variant Primary Progressive Aphasia, has completed, sponsored by Massachusetts General Hospital.

COMPLETED
Registry status
NA
Development phase
10 participants
Enrollment target
1
Study location

Study Summary

Primary Progressive Aphasia (PPA) is a progressive syndrome in the family of Alzheimer's disease and related disorders involving devastating language impairments caused by selective neurodegeneration of the brain's language network. Unfortunately, there is no treatment for PPA. An exciting possibility for treatment is non-invasive repetitive transcranial brain stimulation (rTMS), which induces electric currents in degenerating brain networks, making them in some cases more efficient. Therapeutic benefits from rTMS have been demonstrated when it is applied in many sequential sessions. For example, repeated sessions of rTMS to left dorsolateral prefrontal cortex (dlPFC) is approved by the US Food and Drug administration as a treatment for major depressive disorder. With respect to language, high frequency rTMS increases the response rate for picture naming in healthy individuals and in patients with Alzheimer's disease. Further, in a sham controlled study, Cotelli and colleagues demonstrated that in a group of 10 non-fluent PPA patients, high frequency rTMS over the left and right dlPFC improved the percent of correct responses for action naming. When rTMS was applied for five consecutive days in a sham controlled single case study, Finocchiaro and colleagues showed lasting improvements in language (up to 1 week) in a patient with non-fluent PPA. Trebbastoni and colleagues further showed the same lasting improvements in language (up to 1 week) in a patient with logopenic PPA. Recently, in a sham controlled single case study, Bereau and colleagues applied a more intense rTMS protocol for ten consecutive days and demonstrated significant linguistic improvements in a logopenic PPA patient that lasted for 1 month. These studies have contributed valuable insights into the potential use of rTMS in treating the language symptoms of PPA patients.

Interventions

  • DEVICE Active rTMS
  • DEVICE SHAM rTMS

Study Locations (1)

Massachusetts

  • Massachusetts General Hospital - Boston

Trial Details

FieldValue
Enrollment Target 10 participants
Start Date 2022-03-01
Est. Completion 2024-08-25
Phase NA

Sponsor

Massachusetts General Hospital

2,032 total trials

What the Registry Record Tells You About NCT04188067

The ClinicalTrials.gov registry entry for NCT04188067 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 10 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Massachusetts General Hospital, which has 2,032 total studies on file at ClinicalTrials.gov.

The record links to 3 conditions, with Logopenic Variant Primary Progressive Aphasia appearing as the primary indexed condition, and to 2 interventions - of which Active rTMS is the first listed.

NCT04188067 reports 1 study location spanning 1 distinct geographic area - top geographies include Massachusetts.

Frequently Asked Questions

What is clinical trial NCT04188067 about?

NCT04188067 is a clinical study titled "TMS for the Treatment of Primary Progressive Aphasia". Primary Progressive Aphasia (PPA) is a progressive syndrome in the family of Alzheimer's disease and related disorders involving devastating language impairments caused by selective neurodegeneration of the brain's language network. Unfortunately, there is no treatment for PPA. An exciting possibili...

What is the current status of trial NCT04188067?

This trial is currently completed. It is a NA study. The enrollment target is 10 participants. The study started on 2022-03-01. Estimated completion is 2024-08-25.

What conditions does trial NCT04188067 study?

This clinical trial studies the following conditions: Logopenic Variant Primary Progressive Aphasia, Non-fluent Variant Primary Progressive Aphasia, Semantic Variant Primary Progressive Aphasia.

What interventions are being tested in trial NCT04188067?

The interventions under investigation include: Active rTMS (DEVICE), SHAM rTMS (DEVICE).

Who is sponsoring clinical trial NCT04188067?

This trial is sponsored by Massachusetts General Hospital, which has 2,032 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT04188067 being conducted?

This trial has 1 study location across Massachusetts. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Logopenic Variant Primary Progressive Aphasia

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.