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NCT05860647 · ClinicalTrials.gov registry record · NA

Transmagnetic Stimulation Pilot in Primary Progressive Aphasia

A NA study, sponsored by HealthPartners Institute.

Completed
Registry status
NA
Development phase
3
Enrollment target

NCT05860647 is a NA study that has completed, run by HealthPartners Institute. The registered enrollment target is 3 participants.

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The verdict

NCT05860647, a NA study, has completed, sponsored by HealthPartners Institute.

COMPLETED
Registry status
NA
Development phase
3 participants
Enrollment target

Study Summary

Frontotemporal degeneration (FTD) is a non-Alzheimer's dementia that is the 2nd most common cause of dementia in the United States. FTD may present with focal language symptoms that are clinically described as primary progressive aphasia (PPA). There are two types of PPA associated with FTD-semantic variant primary progressive aphasia (SV-PPA) and nonfluent/agrammatic variant primary progressive aphasia (NFV-PPA). Both diseases are progressive neurodegenerative disease processes that compromise dominant hemisphere large scale brain network function, ultimately resulting in mutism. There are currently no FDA-approved treatments for PPA and management is mostly supportive. In combination with resting state functional MRI (rs-fMRI), transcranial magnetic stimulation (TMS) with intermittent theta burst stimulation (iTBS) offers a non-invasive alternative to pharmacotherapy in persons with PPA. In our prior studies of Alzheimer's disease (AD) and Lewy body Dementia (LBD) subjects, investigators have determined that the anterior temporal pole (area TGd and TGv) is an area that is commonly dysfunctional in dementia. The investigators have already embarked upon an fMRI guided study of iTBS in early stage Alzheimer's disease where subjects received a series of 5 treatments to distinct brain regions inclusive of area TGd. The investigators propose a case study of 3 PPA studies where rs-fMRI is applied to the large-scale language networks.

Interventions

  • DEVICE Intermittent theta burst stimulation

Trial Details

FieldValue
Enrollment Target 3 participants
Start Date 2023-10-02
Est. Completion 2024-05-03
Phase NA

Sponsor

HealthPartners Institute

146 total trials

What the Registry Record Tells You About NCT05860647

The ClinicalTrials.gov registry entry for NCT05860647 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 3 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is HealthPartners Institute, which has 146 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 1 intervention - of which Intermittent theta burst stimulation is the first listed.

NCT05860647 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT05860647 about?

NCT05860647 is a clinical study titled "Transmagnetic Stimulation Pilot in Primary Progressive Aphasia". Frontotemporal degeneration (FTD) is a non-Alzheimer's dementia that is the 2nd most common cause of dementia in the United States. FTD may present with focal language symptoms that are clinically described as primary progressive aphasia (PPA). There are two types of PPA associated with FTD-semantic...

What is the current status of trial NCT05860647?

This trial is currently completed. It is a NA study. The enrollment target is 3 participants. The study started on 2023-10-02. Estimated completion is 2024-05-03.

What interventions are being tested in trial NCT05860647?

The interventions under investigation include: Intermittent theta burst stimulation (DEVICE).

Who is sponsoring clinical trial NCT05860647?

This trial is sponsored by HealthPartners Institute, which has 146 total clinical trials registered on ClinicalTrials.gov.

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.