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Safety and Feasibility of DBS for Bipolar Depression

3. august 2026 oppdatert av: Helen Mayberg, MD, Icahn School of Medicine at Mount Sinai

Deep Brain Stimulation for Bipolar Depression: Assessing the Safety and Use of Intracranial Neurophenotyping of State Switches

This study addresses a critical unmet need in the treatment of bipolar disorder by investigating whether Subcallosal Cingulate (SCC) Deep Brain Stimulation (DBS) can safely and effectively treat treatment-resistant bipolar depression without inducing manic switches. The researchers propose to accomplish this by incorporating monitoring of the SCC local field potentials (LFP) for depression tracking and amygdala LFP monitoring for mania prediction while treating Bipolar I patients with SCC DBS Stimulation. This approach could establish a new paradigm for personalized neuromodulation therapy that uses real-time neural monitoring to optimize outcomes while minimizing risks. By incorporating bilateral, dual-site LFP monitoring from both the SCC and amygdala, this research will allow the researchers to assess the therapeutic efficacy of continuous SCC-DBS and develop novel safety biomarkers that could transform the clinical management of DBS therapy in psychiatry. The findings will have immediate implications for clinical practice and will advance the study team's fundamental understanding of the neural circuits underlying mood regulation and dysregulation in bipolar disorder.

Studieoversikt

Status

Rekruttering

Studietype

Intervensjonell

Registrering (Antatt)

5

Fase

  • Ikke aktuelt

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiekontakt

Studer Kontakt Backup

Studiesteder

    • New York
      • New York, New York, Forente stater, 10019
        • Rekruttering
        • Center for Advanced Circuit Therapeutics, Clinical Neurosciences Center, Mount Sinai West

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

  • Voksen
  • Eldre voksen

Tar imot friske frivillige

Nei

Beskrivelse

Inclusion Criteria:

  • Age 22-70 years
  • Ability to provide written informed consent
  • Primary diagnosis of Bipolar I Disorder confirmed by SCID-5
  • Current major depressive episode (MDE) of at least 12 months duration
  • Stable control of mania for a minimum of 1 year
  • Agreement to remain on current anti-mania medication regimen
  • Hamilton Depression Rating Scale-17 (HDRS-17) score ≥20 at screening and baseline
  • Young Mania Rating Scale (YMRS) score <12 at screening and baseline
  • Treatment-resistant depression: failure to respond to at least 4 adequate trials of antidepressant treatment in the current episode. Antidepressant treatments include: Medications (Must include 2 antidepressant medications from different pharmacological classes), Psychotherapy, ECT, repetitive transcranial magnetic stimulation (rTMS), IV ketamine or intra-nasal esketamine.
  • All patients must be receiving at least one mood stabilizing medication at entry into the trial. Medication regimen must be stable for a minimum of 4 weeks before the baseline visit.
  • Able to provide informed consent
  • English-speaking
  • Deemed suitable surgical candidate by neurosurgical evaluation
  • Under care of treating psychiatrist willing to collaborate with study team
  • Able to reside in New York Metropolitan area during first 6 months or willing/able to travel monthly to study site
  • Provision of at least two emergency contacts age ≥22 residing within reasonable proximity

Exclusion Criteria

  • Current manic or hypomanic episode (YMRS ≥12)
  • Rapid cycling pattern (≥4 mood episodes in the past 12 months)
  • Active suicidal ideation with intent or plan
  • Suicide attempt within six months prior to baseline
  • Current psychotic symptoms
  • Primary diagnosis of schizophrenia, schizoaffective disorder, or other psychotic disorder
  • History (current and/or lifetime) of one or more schizophrenia-spectrum or other psychotic disorders including: schizophrenia, schizoaffective disorder, schizophreniform disorder, delusional disorder, and major depressive disorder with psychosis (unipolar or bipolar), and/or psychotic depression (unipolar or bipolar) (does not include psychosis occurring in the context of a manic episode of a subject with bipolar disorder)
  • Substance use disorder (moderate or severe) within 6 months
  • Presence of any type of dementia / Major Neurocognitive Disorder / significant cognitive impairment interfering with study participation
  • Subject has had a prior VNS Therapy or deep brain stimulation (DBS) implant
  • Subject has a diagnosis of Substance Use Disorder as defined by the DSM-V without sustained remission (12 months or longer)
  • History of borderline or severe personality disorder, as determined by clinical judgment, which would significantly interfere with a subject's participation in the study
  • Active primary diagnosis of one or more of the following disorders: obsessive-compulsive disorder, eating disorder, or post-traumatic stress disorder
  • Cognitive or psychiatric deficit (e.g., amnesia, delirium) that in the investigator's judgment would interfere with the subject's ability to accurately complete study assessments
  • Current or lifetime history of psychotic features in any major depressive episode (MDE)
  • Treatment with another investigational device or investigational drugs
  • Contraindications to MRI (metallic implants, claustrophobia unmanageable with anxiolytics)
  • Contraindications to general anesthesia or neurosurgery
  • Significant structural brain abnormalities precluding safe electrode placement
  • Active infection or immunocompromised state
  • Active unstable medial condition (diabetes, heart disease, hypertension, cancer, endocrine)
  • BMI >35; and/or CRP >3
  • Coagulopathy or anticoagulation that cannot be safely interrupted
  • Pregnancy or planning pregnancy during study period
  • Women of childbearing potential unwilling to use effective contraception
  • Prisoners or institutionalized individuals
  • Decisionally impaired individuals (unless previously consented when capacitated)
  • Special status patients (employees, VIPs, celebrities, public figures) unless consented before special status known

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Behandling
  • Tildeling: N/A
  • Intervensjonsmodell: Enkeltgruppeoppdrag
  • Masking: Ingen (Open Label)

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Eksperimentell: Participants with Bipolar disorder
Participants with BPD will be treated with open label active bilateral Subcallosal Cingulate (SCC) Deep Brain Stimulation (DBS) with ongoing local field potential monitoring from the SCC and amygdala.
Open label active Deep Brain Stimulation (DBS) with continuous monitoring of local field potentials (LFP) from the SCC and amygdala.

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Hamilton Depression Rating Scale (HDRS)
Tidsramme: Baseline and weekly up to 1 year
The Hamilton Depression Rating Scale (HDRS), is a 17-item questionnaire assessing severity of depression. Scores range from 0-50, with a higher score indicating more severe depression.
Baseline and weekly up to 1 year

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Young Mania Rating Scale (YMRS)
Tidsramme: Baseline and weekly up to 1 year
Young Mania Rating Scale (YMRS) is an 11-item questionnaire to measure the severity of manic symptoms. 7 items are scored 0-4 and the other 4 items are scored 0-8. The overall YMRS score ranges from 0-60, with a higher score indicating more severe mania.
Baseline and weekly up to 1 year

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Etterforskere

  • Hovedetterforsker: Helen Mayberg, MD, Icahn School of Medicine at Mount Sinai

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart (Antatt)

1. august 2026

Primær fullføring (Antatt)

1. oktober 2028

Studiet fullført (Antatt)

1. oktober 2028

Datoer for studieregistrering

Først innsendt

29. juli 2026

Først innsendt som oppfylte QC-kriteriene

3. august 2026

Først lagt ut (Faktiske)

4. august 2026

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

4. august 2026

Siste oppdatering sendt inn som oppfylte QC-kriteriene

3. august 2026

Sist bekreftet

1. august 2026

Mer informasjon

Begreper knyttet til denne studien

Andre studie-ID-numre

  • STUDY-26-00089
  • DG251219 (Annet stipend/finansieringsnummer: Breakthrough Discoveries for thriving with Bipolar Disorder)

Plan for individuelle deltakerdata (IPD)

Planlegger du å dele individuelle deltakerdata (IPD)?

JA

IPD-planbeskrivelse

Individual participant demographic and outcome data, after deidentification.

IPD-delingstidsramme

Beginning 9 months and ending 36 months following publication of findings.

Tilgangskriterier for IPD-deling

Investigators whose proposed use of the data has been approved by an independent review committee ('learned intermediary') identified for this purpose.

To achieve aims in the approved proposal, physiology and imaging data will be housed at a URL to be created during the protocol. After publication the URL will be provided and investigators whose proposed use of the data has been approved will be provided with access.

IPD-deling Støtteinformasjonstype

  • STUDY_PROTOCOL
  • ICF
  • CSR

Legemiddel- og utstyrsinformasjon, studiedokumenter

Studerer et amerikansk FDA-regulert medikamentprodukt

Nei

Studerer et amerikansk FDA-regulert enhetsprodukt

Ja

produkt produsert i og eksportert fra USA

Nei

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