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Pain Alleviation for Patients Receiving Directional Deep Brain Stimulation to Treat Neuropathic Dental Pain

Status: Recruiting
Location: See location...
Intervention Type: Device
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

This prospective observational study will evaluate pain outcomes in patients with neuropathic dental pain (Atypical Odontalgia/Phantom Tooth Pain) who undergo directional deep brain stimulation (DBS). Participants will complete validated pain, disability, quality-of-life, and mood assessments before surgery and following DBS programming. Directional stimulation will be applied to different thalamic targets to determine whether specific stimulation settings are associated with greater pain relief. The study aims to characterize changes in pain and quality of life following DBS and to identify the stimulation target associated with the greatest reduction in neuropathic dental pain.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 19
Maximum Age: 80
Healthy Volunteers: f
View:

• Age 19 to 80 years.

• Diagnosis of Atypical Odontalgia (AO) (also known as neuropathic dental pain).

• Receiving deep brain stimulation (DBS) treatment for AO due to inadequate response to conventional therapies, including: Pharmacological therapies, and/or Local anesthetics, corticosteroid injections, or nerve blocks.

• Able and willing to provide informed consent.

Locations
Other Locations
Canada
Vancouver General Hospital
RECRUITING
Vancouver
Contact Information
Primary
Danielle Pietramala
danielle.pietram@ubc.ca
604-875-4111
Time Frame
Start Date: 2026-01-01
Estimated Completion Date: 2028-01-01
Participants
Target number of participants: 5
Treatments
Experimental: Ring-Mode Stimulation
Participants receive DBS ring-mode stimulation, allowing current to spread across the target region encompassing the ventral posteromedial nucleus (VPM), anterior pulvinar (aPu), and centromedian nucleus (CM).
Experimental: Ventral Posteromedial Nucleus (VPM) Stimulation
Participants receive directional DBS stimulation targeted toward the ventral posteromedial nucleus (VPM) of the thalamus.
Experimental: Anterior Pulvinar (aPu) Stimulation
Participants receive directional DBS stimulation targeted toward the anterior pulvinar (aPu) of the thalamus.
Experimental: Centromedian Nucleus (CM) Stimulation
Participants receive directional DBS stimulation targeted toward the centromedian nucleus (CM) of the thalamus.
No_intervention: Stimulation Off
Participants have the DBS device turned off and serve as a control condition for comparison with active stimulation settings.
Related Therapeutic Areas
Sponsors
Leads: University of British Columbia

This content was sourced from clinicaltrials.gov