Trials / Active Not Recruiting
Active Not RecruitingNCT06485687
Low Intensity Focused Ultrasound for Binge Eating Disorder
Early Feasibility Study of Low-Intensity Focused Ultrasound (LIFU) Neuromodulation in Patients With Binge Eating Disorder (BED)
- Status
- Active Not Recruiting
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 15 (estimated)
- Sponsor
- Ali Rezai · Academic / Other
- Sex
- All
- Age
- 22 Years – 65 Years
- Healthy volunteers
- Not accepted
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)
Detailed description
The primary objective is to evaluate the safety, feasibility and tolerability of LIFU as an adjunct neuromodulatory treatment for BED
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | LIFU Neuromodulation | Subjects will undergo a single LIFU of the target brain region |
Timeline
- Start date
- 2024-10-31
- Primary completion
- 2026-12-31
- Completion
- 2027-12-31
- First posted
- 2024-07-03
- Last updated
- 2025-12-18
Locations
1 site across 1 country: United States
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT06485687. Inclusion in this directory is not an endorsement.