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NCT07220005 · ClinicalTrials.gov registry record · NA

Low Intensity Focused Ultrasound Stimulation in Stroke Patients - Parameter Optimization

A NA study of Stroke and Arm Weakness as a Consequence of Stroke, sponsored by Duke University.

Recruiting
Registry status
NA
Development phase
24
Enrollment target
1
Study location

NCT07220005 is a NA study of Stroke and Arm Weakness as a Consequence of Stroke that is actively recruiting participants, run by Duke University. The registered enrollment target is 24 participants, below the 12,016-participant average among 454 other Stroke trials with a reported enrollment target (100% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT07220005, a NA study of Stroke and Arm Weakness as a Consequence of Stroke, is actively recruiting participants, sponsored by Duke University.

RECRUITING
Registry status
NA
Development phase
24 participants
Enrollment target
1
Study location

Study Summary

The goal of this research study is to optimize the parameter of Low-Intensity Focused Ultrasound Stimulation (LIFUS) that is most effective in changing cortical excitability and motor learning skills in patients who suffered a stroke. The researchers hope to answer two questions. * with increasing power, would LIFUS be more effective? * with the same power, what LIFUS timing is the best For Aim 1, the study will compare 8, 4 W/cm\^2 to a zero(sham) stimulation to see if higher power is the better. For Aim 2, the study will compare 500 vs 1000 vs 2000 Hz "timing" to see which one is better.

Interventions

  • DEVICE Low intensity focused ultrasound stimulation

Study Locations (1)

North Carolina

  • Duke University Hospital - Durham

Trial Details

FieldValue
Enrollment Target 24 participants
Start Date 2025-12-10
Est. Completion 2026-06-30
Phase NA

Sponsor

Duke University

1,725 total trials

What the Registry Record Tells You About NCT07220005

The ClinicalTrials.gov registry entry for NCT07220005 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 24 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 12,016-participant average among 454 other Stroke trials with a reported enrollment target (100% lower). The listed sponsor is Duke University, which has 1,725 total studies on file at ClinicalTrials.gov.

The record links to 5 conditions, with Stroke appearing as the primary indexed condition, and to 1 intervention - of which Low intensity focused ultrasound stimulation is the first listed.

NCT07220005 reports 1 study location spanning 1 distinct geographic area - top geographies include North Carolina.

Frequently Asked Questions

What is clinical trial NCT07220005 about?

NCT07220005 is a clinical study titled "Low Intensity Focused Ultrasound Stimulation in Stroke Patients - Parameter Optimization". The goal of this research study is to optimize the parameter of Low-Intensity Focused Ultrasound Stimulation (LIFUS) that is most effective in changing cortical excitability and motor learning skills in patients who suffered a stroke. The researchers hope to answer two questions. * with increasing ...

What is the current status of trial NCT07220005?

This trial is currently recruiting. It is a NA study. The enrollment target is 24 participants. The study started on 2025-12-10. Estimated completion is 2026-06-30.

What conditions does trial NCT07220005 study?

This clinical trial studies the following conditions: Stroke, Arm Weakness as a Consequence of Stroke, Upper Extremity Impairments, Upper Extremity Weakness, Upper Extremity Hemiparesis.

What interventions are being tested in trial NCT07220005?

The interventions under investigation include: Low intensity focused ultrasound stimulation (DEVICE).

Who is sponsoring clinical trial NCT07220005?

This trial is sponsored by Duke University, which has 1,725 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT07220005 being conducted?

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

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