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Low Intensity Focused Ultrasound for Binge Eating Disorder

NCT06485687 · Status: ACTIVE_NOT_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 15

Last updated 2025-12-18

No results posted yet for this study

Summary

This study is a prospective, single-center, single-arm early feasibility study, to establish safety and tolerability of LIFU for neuromodulation in patients with Binge Eating Disorder (BED)

Conditions

  • Binge-Eating Disorder

Interventions

DEVICE

LIFU Neuromodulation

Subjects will undergo a single LIFU of the target brain region

Sponsors & Collaborators

  • Ali Rezai

    lead OTHER

Principal Investigators

  • Ali Rezai · WVU Rockefeller Neuroscience Institute

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
22 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-10-31
Primary Completion
2026-12-31
Completion
2027-12-31
FDA Device
Yes

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06485687 on ClinicalTrials.gov