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Recruiting NCT07410598

NCT07410598 Safety and Tolerability of Patterned Stimulation for DBS in the Home Setting

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Clinical Trial Summary
NCT ID NCT07410598
Status Recruiting
Phase
Sponsor University of Florida
Condition Parkinson Disease
Study Type INTERVENTIONAL
Enrollment 60 participants
Start Date 2026-05-06
Primary Completion 2028-03-01

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age 80 Years
Study Type INTERVENTIONAL
Interventions
Biphasic deep brain stimulationConventional deep brain stimulationTheta burst deep brain stimulation

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 60 participants in total. It began in 2026-05-06 with a primary completion date of 2028-03-01.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

The primary objective of the proposed pilot study is to assess the safety and tolerability of active patterned Deep Brain Stimulation (pDBS) when administered in a home setting for patients with Parkinson's disease (PD) who have had stable bilateral Subthalamic Nucleus (STN) and Globus Pallidus internus (GPi) DBS.

Eligibility Criteria

Inclusion Criteria: * Bilateral STN or GPi DBS with Boston Scientific Vercise Genus DBS System * Diagnosis of Parkinson's disease as confirmed by a movement disorders fellowship trained neurologist * Chronic stable DBS therapy, defined as having DBS therapy for at least 6 months Exclusion Criteria: * History of previous neurosurgical intervention aside from DBS * Diagnosis of dementia (whether primary or related to Parkinson's disease) * A diagnosis of atypical parkinsonism or secondary parkinsonism at any time after DBS implantation

Contact & Investigator

Central Contact

Joshua Wong, MD

✉ joshua.wong@neurology.ufl.edu

📞 352-294-5400

Frequently Asked Questions

Who can join the NCT07410598 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, up to 80 Years, studying Parkinson Disease. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07410598 currently recruiting?

Yes, NCT07410598 is actively recruiting participants. Contact the research team at joshua.wong@neurology.ufl.edu for enrollment information.

Where is the NCT07410598 trial being conducted?

This trial is being conducted at Gainesville, United States.

Who is sponsoring the NCT07410598 clinical trial?

NCT07410598 is sponsored by University of Florida. The trial plans to enroll 60 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: July 2026  ·  Data Methodology