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Recruiting NCT07348705

NCT07348705 Electrophysiology-based DBS Programming for PD

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Clinical Trial Summary
NCT ID NCT07348705
Status Recruiting
Phase
Sponsor University of Florida
Condition Parkinson's Disease (PD)
Study Type INTERVENTIONAL
Enrollment 30 participants
Start Date 2026-01-15
Primary Completion 2027-01-15

Eligibility & Interventions

Sex All sexes
Min Age 21 Years
Max Age 89 Years
Study Type INTERVENTIONAL
Interventions
Clinician-based DBS programmingMaximum Beta power-based DBS programmingBroad-band electrophysiology-based DBS programming

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 30 participants in total. It began in 2026-01-15 with a primary completion date of 2027-01-15.

⚠ 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

Deep brain stimulation (DBS) effectively alleviates motor symptoms in Parkinson's disease (PD). However, current programming is manual and time-consuming. This study will evaluate physiology-based programming using local field potentials (LFPs) to identify optimal stimulation parameters. Specifically, DBS contact selection based on beta power and a broad-band approach will be compared with conventional clinician-based programming.

Eligibility Criteria

Inclusion Criteria: * Patients with a diagnosis of idiopathic PD fulfilling the Movement Disorder Society Clinical Diagnostic Criteria for PD * DBS implantation with the Percept DBS device (Medtronic, USA) for the treatment of motor symptoms * Ability to give informed consent for the study * Willingness to do this study at the time of the initial programming session * Age 21 to 89 years old Exclusion Criteria: * Inability to comply with the study protocol * Atypical Parkinsonism * Any personality or mood symptoms that study personnel believe will interfere with the study requirements

Contact & Investigator

Central Contact

Joshua Wong, MD

✉ Joshua.Wong@neurology.ufl.edu

📞 352-294-5400

Principal Investigator

Joshua Wong, MD

PRINCIPAL INVESTIGATOR

University of Florida

Frequently Asked Questions

Who can join the NCT07348705 clinical trial?

This trial is open to participants of all sexes, aged 21 Years or older, up to 89 Years, studying Parkinson's Disease (PD). Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07348705 currently recruiting?

Yes, NCT07348705 is actively recruiting participants. Contact the research team at Joshua.Wong@neurology.ufl.edu for enrollment information.

Where is the NCT07348705 trial being conducted?

This trial is being conducted at Gainesville, United States.

Who is sponsoring the NCT07348705 clinical trial?

NCT07348705 is sponsored by University of Florida. The principal investigator is Joshua Wong, MD at University of Florida. The trial plans to enroll 30 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: April 2026  ·  Data Methodology