- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT07671950
Neuropathic Dental Pain & DBS
Pain Alleviation for Patients Receiving Directional Deep Brain Stimulation to Treat Neuropathic Dental Pain
Studieoversigt
Status
Betingelser
Intervention / Behandling
Detaljeret beskrivelse
Neuropathic dental pain, also known as Atypical Odontalgia (AO) or Phantom Tooth Pain (PTP), is a chronic pain condition characterized by persistent tooth or facial pain in the absence of identifiable dental pathology. The condition is thought to result from injury to peripheral nerve structures that leads to alterations in central pain processing. Standard treatments, including antidepressants, neuroleptic medications, local anesthetic injections, corticosteroids, and nerve blocks, may provide relief for some patients; however, a subset of patients continue to experience debilitating pain despite these interventions.
Deep brain stimulation (DBS) is an established neurosurgical therapy for several neurological disorders and has been used off-label for the treatment of chronic neuropathic pain. Previous studies suggest that stimulation of thalamic structures involved in pain processing, including the ventral posteromedial nucleus (VPM), centromedian nucleus (CM), and anterior pulvinar (aPu), may provide pain relief for neuropathic facial pain. However, no established DBS target currently exists for neuropathic dental pain.
This prospective observational study will evaluate pain outcomes in patients with neuropathic dental pain who undergo directional DBS. Directional DBS leads will be implanted in a location that permits stimulation of the VPM, CM, and aPu regions of the thalamus. Following surgery, participants will undergo routine clinical programming during which stimulation settings will be systematically adjusted to direct stimulation toward each target region, as well as ring-mode stimulation and an off-stimulation condition. Participants will remain blinded to the stimulation settings.
Participants will complete validated measures of pain, pain-related disability, quality of life, and depressive symptoms before surgery and after completion of the programming period. Visual Analog Scale (VAS) pain ratings will also be collected following each stimulation condition to evaluate differences in pain relief between targets. The primary objective is to assess changes in pain levels associated with different stimulation settings and identify the stimulation target associated with the greatest reduction in neuropathic dental pain. Secondary objectives include evaluating changes in pain-related disability, quality of life, and mood following DBS treatment.
The findings from this study will provide preliminary evidence regarding optimal thalamic stimulation targets for neuropathic dental pain and may inform future research and treatment approaches for patients with this challenging and currently underserved condition.
Undersøgelsestype
Tilmelding (Anslået)
Fase
- Ikke anvendelig
Kontakter og lokationer
Studiekontakt
- Navn: Danielle Pietramala
- Telefonnummer: 68396 604-875-4111
- E-mail: danielle.pietram@ubc.ca
Studiesteder
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British Columbia
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Vancouver, British Columbia, Canada, V5Z1M9
- Rekruttering
- Vancouver General Hospital
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Kontakt:
- Danielle Pietramala
- Telefonnummer: 6043495059
- E-mail: d.pietramala@hotmail.com
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-
Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
- Voksen
- Ældre voksen
Tager imod sunde frivillige
Beskrivelse
Inclusion Criteria:
- 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.
Exclusion Criteria:
- Refusal or inability to provide informed consent.
- Known major depression.
- Acute psychosis.
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: Randomiseret
- Interventionel model: Crossover opgave
- Maskning: Dobbelt
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
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Eksperimentel: 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).
|
Participants will receive standard-of-care directional deep brain stimulation (DBS) using an implanted DBS system.
Stimulation will be delivered using ring-mode stimulation, directional stimulation toward the ventral posteromedial nucleus (VPM), anterior pulvinar (aPu), or centromedian nucleus (CM), or with stimulation turned off.
Participants will undergo each stimulation condition in a randomized sequence.
|
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Eksperimentel: Ventral Posteromedial Nucleus (VPM) Stimulation
Participants receive directional DBS stimulation targeted toward the ventral posteromedial nucleus (VPM) of the thalamus.
|
Participants will receive standard-of-care directional deep brain stimulation (DBS) using an implanted DBS system.
Stimulation will be delivered using ring-mode stimulation, directional stimulation toward the ventral posteromedial nucleus (VPM), anterior pulvinar (aPu), or centromedian nucleus (CM), or with stimulation turned off.
Participants will undergo each stimulation condition in a randomized sequence.
|
|
Eksperimentel: Anterior Pulvinar (aPu) Stimulation
Participants receive directional DBS stimulation targeted toward the anterior pulvinar (aPu) of the thalamus.
|
Participants will receive standard-of-care directional deep brain stimulation (DBS) using an implanted DBS system.
Stimulation will be delivered using ring-mode stimulation, directional stimulation toward the ventral posteromedial nucleus (VPM), anterior pulvinar (aPu), or centromedian nucleus (CM), or with stimulation turned off.
Participants will undergo each stimulation condition in a randomized sequence.
|
|
Eksperimentel: Centromedian Nucleus (CM) Stimulation
Participants receive directional DBS stimulation targeted toward the centromedian nucleus (CM) of the thalamus.
|
Participants will receive standard-of-care directional deep brain stimulation (DBS) using an implanted DBS system.
Stimulation will be delivered using ring-mode stimulation, directional stimulation toward the ventral posteromedial nucleus (VPM), anterior pulvinar (aPu), or centromedian nucleus (CM), or with stimulation turned off.
Participants will undergo each stimulation condition in a randomized sequence.
|
|
Ingen indgriben: Stimulation Off
Participants have the DBS device turned off and serve as a control condition for comparison with active stimulation settings.
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Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
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Pain Severity Measured by Visual Analogue Scale (VAS)
Tidsramme: Baseline (pre-operative); after each 2-week stimulation period during the 10-week post-activation programming phase; and 3 months after completion of the randomized stimulation period.
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Pain severity will be assessed using the Visual Analogue Scale (VAS).
Participants will complete the VAS following two weeks on each of five stimulation settings (ring mode, VPM, aPu, CM, and off stimulation).
The primary outcome is the comparison of VAS scores across stimulation settings to identify the setting associated with the greatest pain reduction.
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Baseline (pre-operative); after each 2-week stimulation period during the 10-week post-activation programming phase; and 3 months after completion of the randomized stimulation period.
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Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Change in Pain Severity Assessed by the Short-Form McGill Pain Questionnaire-2 (SF-MPQ-2)
Tidsramme: Baseline (pre-operative) and 3 months after completion of the randomized stimulation period.
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Pain characteristics and severity will be assessed using the SF-MPQ-2.
Changes from baseline to follow-up will be evaluated.
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Baseline (pre-operative) and 3 months after completion of the randomized stimulation period.
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Change in Pain-Related Disability Assessed by the Pain Disability Index (PDI)
Tidsramme: Baseline (pre-operative) and 3 months after completion of the randomized stimulation period.
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The impact of pain on daily functioning will be measured using the Pain Disability Index.
Changes from baseline to follow-up will be evaluated.
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Baseline (pre-operative) and 3 months after completion of the randomized stimulation period.
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Change in Health-Related Quality of Life Assessed by the 36-Item Short Form Survey (SF-36)
Tidsramme: Baseline (pre-operative) and 3 months after completion of the randomized stimulation period.
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Health-related quality of life will be measured using the SF-36 questionnaire.
Changes from baseline to follow-up will be evaluated.
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Baseline (pre-operative) and 3 months after completion of the randomized stimulation period.
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Change in Depressive Symptoms Assessed by the Beck Depression Inventory (BDI)
Tidsramme: Baseline (pre-operative) and 3 months after completion of the randomized stimulation period.
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Depressive symptoms will be measured using the Beck Depression Inventory.
Changes from baseline to follow-up will be evaluated.
|
Baseline (pre-operative) and 3 months after completion of the randomized stimulation period.
|
|
Change in Pain Severity Assessed by the Visual Analogue Scale (VAS)
Tidsramme: Baseline (pre-operative) and 3 months after completion of the randomized stimulation period.
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Overall pain intensity will be compared between baseline and follow-up while participants are maintained on their optimal stimulation setting.
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Baseline (pre-operative) and 3 months after completion of the randomized stimulation period.
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Samarbejdspartnere og efterforskere
Sponsor
Datoer for undersøgelser
Studer store datoer
Studiestart (Faktiske)
Primær færdiggørelse (Anslået)
Studieafslutning (Anslået)
Datoer for studieregistrering
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først opslået (Faktiske)
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Andre undersøgelses-id-numre
- H24-01903
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
Studerer et amerikansk FDA-reguleret lægemiddelprodukt
Studerer et amerikansk FDA-reguleret enhedsprodukt
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