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RECRUITING NA

Pulsed Electromagnetic Field Treatment With Dementia Patients

NCT06862557 · View on ClinicalTrials.gov ↗

Study Summary

An open label pilot study in mild to moderate AD/ADRD patients to assess the effects of treatment with ECHS AD/ADRD pulsed electromagnetic treatment device on disease progression. Enrolled patients will receive active devices. They will treat themselves at home three times a day for 15 minutes over 120 days. Primary end point is the The Alzheimer's Disease Assessment Scale-Cognitive Subscale. Participants will be followed-up for 9 months post-treatment.

Interventions

  • DEVICE ECHS AD Device

Study Locations (1)

Florida

  • University of Miami — Boca Raton

Trial Details

FieldValue
Enrollment Target 48 participants
Start Date 2025-04-01
Est. Completion 2026-09-30
Phase NA

Sponsor

Herrick Medical

29 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06862557

The ClinicalTrials.gov registry entry for NCT06862557 describes a study currently listed as recruiting. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 48 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Herrick Medical, which has 29 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 3 conditions, with Alzheimer's Disease appearing as the primary indexed condition, and to 1 intervention — of which ECHS AD Device is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT06862557 reports 1 study location spanning 1 distinct geographic area — top geographies include Florida. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT06862557 about?

NCT06862557 is a clinical study titled "Pulsed Electromagnetic Field Treatment With Dementia Patients". An open label pilot study in mild to moderate AD/ADRD patients to assess the effects of treatment with ECHS AD/ADRD pulsed electromagnetic treatment device on disease progression. Enrolled patients will receive active devices. They will treat themselves at home three times a day for 15 minutes over ...

What is the current status of trial NCT06862557?

This trial is currently recruiting. It is a NA study. The enrollment target is 48 participants. The study started on 2025-04-01. Estimated completion is 2026-09-30.

What conditions does trial NCT06862557 study?

This clinical trial studies the following conditions: Alzheimer's Disease, Vascular Dementia, Lewy Body Dementia. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT06862557?

The interventions under investigation include: ECHS AD Device (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT06862557?

This trial is sponsored by Herrick Medical, which has 29 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT06862557 being conducted?

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

Related

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