Using Low Intensity Focused Ultrasound to Modulate Deep Brain Areas for Tremor Control in Parkinson's Disease Patients.

Not Applicable

Active, not recruiting

• Conditions: Parkinson Disease
• Interventions: Device: Low intensity focused ultrasound

• Registration Number: NCT06259708
• Lead Sponsor: University of British Columbia

Brief Summary

Researchers have found that a treatment called Magnetic Resonance guided Focused Ultrasound (MRgFUS) can effectively reduce tremors in patients with essential tremor (ET) and Parkinson's disease (PD). They noticed that ET patients initially responded better to the treatment than PD patients, but by the end of the treatment, both groups showed similar improvement. The study also suggested that targeting a specific area of the brain called the Zona Incerta (ZI) may be more beneficial for PD patients. Based on these findings, the investigators plan to use low-intensity focused ultrasound to directly modulate the ZI area and investigate the mechanisms of reduced tremors in PD patients. The investigators will also compare the effectiveness of this approach with the current target, the ventral intermediate nucleus (Vim) of the thalamus. The investigators will use a simulation model to determine the best ultrasound parameters for this new approach and will also examine the impact of the treatment on the brain's network activity using functional Magnetic Resonance Imaging. Success of this project may lay the foundation for finding a more effective target for MRgFUS treatment of PD tremor.

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2024-01-26
• Study First Submitted QC: 2024-02-13
• Study First Posted: 2024-02-14
• Study Start: 2024-03-01
• Status Verified: 2025-03
• Last Update Submitted: 2025-03-24
• Last Update Posted: 2025-03-27
• Primary Completion: 2025-08-01
• Study Completion: 2025-08-01

Recruitment & Eligibility

• Status: ACTIVE_NOT_RECRUITING
• Sex: All
• Target Recruitment: 20

Inclusion Criteria

• Confirmed diagnosis of Parkinson's disease
• Resting tremor score (MDS-UPDRS III 3.17 Rest Tremore Amplitude (RUE or LUE)) ≥ 2
• Between the ages of 40-80 years
• Hoehn and Yahr stage between 1-3 (mild to moderate PD) in the "ON" state
• Patients who are willing to have a partial (~8 cm diameter circular area above the ear) hair shaving.

Exclusion Criteria

• Atypical Parkinsonism
• History of essential tremor
• Dementia preventing informed consent
• Change in Parkinson's medication with the last 2 weeks
• Neurological disease other than PD, including Alzheimer's disease, multi-infarct dementia, Huntington's disease, normal pressure hydrocephalus, a brain tumor, progressive supranuclear palsy, seizure disorder, subdural hematoma, multiple sclerosis, or history of significant head trauma
• Unstable medical conditions or serious disease/conditions (e.g., cancer undergoing active treatment, poorly controlled diabetes)
• Concurrent treatment for PD with Duodopa
• Concurrent treatment for PD with deep brain stimulation (DBS)
• Thickness of the temporal bone < 7 mm
• Individuals should also not participate if they have any of the following contraindications for undergoing fMRI scanning:
• Cardiac pacemaker, wires, or defibrillator
• Metal in eye or orbit, including the history of any eye injury involving metal fragments and increased risk due to (history of) working as a metal worker (grinding, machining, or welding)
• Ferromagnetic aneurysm clip
• Possibility of pregnancy
• Artificial heart valve
• Ear or eye implant, including cochlear implant
• Brain aneurysm clip
• Implanted drug infusion pump
• Electrical stimulator to nerves or bones
• Coil, catheter, or filter in any blood vessel
• Orthopedic hardware (artificial joint, plate, screw, rod)
• Other metallic prostheses
• Shrapnel, bullets, or other metal fragments
• Surgery, piercings or tattoos (including tattooed eyeliner) in the last six weeks
• Medication releasing skin patches (i.e. nicotine, birth control, nitroglycerine)
• History of claustrophobia

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: CROSSOVER

Arm && Interventions

Group	Intervention	Description
ZI first	Low intensity focused ultrasound	Participants assigned to this arm get LIFU stimulation in the Vim before the ZI.
Vim first	Low intensity focused ultrasound	Participants assigned to this arm get LIFU stimulation in the Vim before the ZI.

Primary Outcome Measures

Name	Time	Method
Tremor	At 50Hz for 40 minutes 30 minutes after intervention	Finger acceleration (mm/s\^2)
Functional connectivity	Once before and once immediately after intervention	fMRI

Trial Locations

Locations (1)

University of British Columbia, DMCBH; 🇨🇦 Vancouver, British Columbia, Canada