Denne siden ble automatisk oversatt og nøyaktigheten av oversettelsen er ikke garantert. Vennligst referer til engelsk versjon for en kildetekst.

Development of Low-Intensity Focused Ultrasound for Post Traumatic Brain Injury Depression

14. september 2026 oppdatert av: Mahendra Bhati, Stanford University

The goal of this clinical trial is to learn about evaluate the safety, tolerability, and feasibility of MRI-guided LIFU targeting the sgACC in Veterans with post-traumatic brain injury depression. The main questions it aims to answer are:

  1. the safety, tolerability, and feasibility of MRI-guided LIFU.
  2. Evaluate preliminary antidepressant efficacy.
  3. Characterize target engagement using multimodal neuroimaging and electrophysiology.
  4. Identify imaging and electrophysiological biomarkers that predict treatment response.
  5. Generate preliminary effect size estimates to support future multicenter clinical trials.

Studieoversikt

Detaljert beskrivelse

The study is a single-site, randomized (3:2 to active LIFU or sham), rater- and participant-blinded mechanistic study of MRI-guided low-intensity focused ultrasound (LI-FUS) targeting the subgenual anterior cingulate cortex (sgACC) in adult Veterans with post traumatic brain injury depression (PTD). The purpose of this study is to evaluate the safety and tolerability of repeated sgACC-targeted LI-FUS stimulation in adult Veterans with PTD. To evaluate the preliminary antidepressant efficacy of repeated sgACC-targeted LI-FUS in adult Veterans with PTD. To characterize the relationship between delivered LI-FUS dose and clinical response in adult Veterans with PTD. To characterize changes in neuroimaging and electrophysiologic measures associated with LI-FUS, including fMRI- and EEG-based indices of target engagement and network modulation, in adult Veterans with PTD. (b) To evaluate whether baseline fMRI and EEG features predict clinical response to LI-FUS in adult Veterans with PTD.

Studietype

Intervensjonell

Registrering (Antatt)

25

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

    • California
      • Stanford, California, Forente stater, 94305
        • Department of Psychiatry and Behavioral Sciences, Stanford School of Medicine
        • Ta kontakt med:
        • Hovedetterforsker:
          • Mahendra Bhati, MD

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

Tar imot friske frivillige

Nei

Beskrivelse

Inclusion Criteria:

  1. Adult Veteran, male or female, 22 to 55 years of age at the time of screening.
  2. Able to read, understand, and provide written, dated informed consent before initiation of formal study screening procedures. A brief IRB-approved telephone pre-screen may be conducted prior to written informed consent as described in Section 8.1. Proficiency in English sufficient to complete questionnaires / follow instructions during fMRI assessments and LIFU interventions. Stated willingness to comply with all study procedures, including availability for the duration of the study, and to communicate with study personnel about adverse events and other clinically important information.
  3. History of non-penetrating mild to moderate TBI confirmed by medical records and adjudicated by the study investigator using established TBI criteria (e.g., ACRM/VA-DoD criteria). If contemporaneous records are incomplete, a structured lifetime TBI interview may be used to support classification.
  4. The TBI must have occurred at least 3 months before the occurrence of depression
  5. Current depressive disorder defined in the Diagnosis and Statistical Manual of Mental Disorders, Fifth Edition, Text Revision (DSM-5).
  6. Medical records confirming a history of moderate to severe treatment-resistance as defined by a score of 7-14 on the Maudsley Staging Method (MSM3).
  7. MADRS score of ≥20 at screening.
  8. Total duration of current depressive episode is less than 2 years
  9. LIFU naive.
  10. Access to ongoing psychiatric care before and after completion of the study.
  11. The dose of the primary antidepressant medication must be stable for 6 weeks prior to baseline , and participants must agree to continue at this dose throughout the study period.
  12. In good general health, as evidenced by medical history.
  13. For females of reproductive potential: use of highly effective contraception for at least 1 month prior to baseline and agreement to use such a method during study participation.
  14. Agreement to adhere to Lifestyle Considerations (see section 5.3) throughout study duration.

Exclusion Criteria:

  1. Any lifetime DSM-5 depressive disorder or clinically significant depressive episode with onset prior to the qualifying index TBI, including major depressive disorder, persistent depressive disorder, or other specified/unspecified depressive disorder, or any antidepressant treatment initiated for depression prior to the index TBI.
  2. Pregnancy
  3. Primary psychiatric condition other than MDD requiring treatment except stable comorbid anxiety disorder
  4. History of or current psychotic disorder or bipolar disorder
  5. Severe borderline personality disorder.
  6. Diagnosis of Intellectual Disability or Autism Spectrum Disorder
  7. Current moderate or severe substance use disorder or demonstrating signs of acute substance withdrawal
  8. Urine screening test positive for illicit substances
  9. Active suicidal ideation (defined as an MSSI > 8) or a suicide attempt (as defined by the C-SSRS) within the past one year
  10. Cognitive impairment (defined as MoCA < 23)

10. Any history of ECT without meeting responder criteria 11. Recent (within 4 weeks of any clinical effect) or concurrent use of rapid acting antidepressant agent (i.e., ketamine or a course of ECT) 12. History of significant neurologic disease, including dementia, Parkinson's or Huntington's disease, brain tumor, seizure disorder, subdural hematoma, or multiple sclerosis 13. Untreated or insufficiently treated endocrine disorder. 14. Contraindication to receiving LIFU 15. Contraindication to MRI (ferromagnetic metal in their body) 16. Treatment with another investigational drug or other intervention within the study period 17. Unstable symptoms between screening and baseline as defined by a > 30% change in MADRS-S score.

18. Any other condition deemed by the PD to interfere with the study or increase risk to the participant

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: Randomisert
  • Intervensjonsmodell: Parallell tildeling
  • Masking: Dobbelt

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Aktiv komparator: Active Low-Intensity Focused Ultrasound (LIFU)
Participants receive active LIFU over 5 consecutive treatment days, with 5 sessions per day and 20 minutes per session
MRI-guided Low-Intensity Focused Ultrasound (LIFU) neuromodulation targeting the sgACC delivered over a brief, intensive course (20-minute sessions; 5 sessions/day for 5 consecutive days).
Sham-komparator: Sham Low-Intensity Focused Ultrasound (LIFU)
Participants receive sham LIFU over 5 consecutive treatment days, with 5 sessions per day and 20 minutes per session
Non-active MRI-guided Low-Intensity Focused Ultrasound (LIFU) neuromodulation targeting the sgACC delivered over a brief, intensive course (20-minute sessions; 5 sessions/day for 5 consecutive days).

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
To evaluate the safety and tolerability of repeated sgACC-targeted LIFU stimulation in adult Veterans with PTD.
Tidsramme: Baseline, Treatment Days 1 through 5, 1-Week, 1-2:4-week follow up visits.
Cumulative incidence of treatment-emergent adverse events and serious adverse events.
Baseline, Treatment Days 1 through 5, 1-Week, 1-2:4-week follow up visits.

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
To evaluate the preliminary antidepressant efficacy of repeated sgACC-targeted LIFU in adult Veterans with PTD.
Tidsramme: Baseline, 1-week follow up, 4-week follow up
Absolute change from baseline in the MADRS total score.
Baseline, 1-week follow up, 4-week follow up

Andre resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
To characterize changes in neuroimaging measures associated with LIFU.
Tidsramme: Baseline and 1-week follow-up
Change from baseline in prespecified resting-state fMRI measures of sgACC-centered functional connectivity and depression-related network connectivity.
Baseline and 1-week follow-up
To characterize changes in electrophysiologic measures associated with LIFU.
Tidsramme: Baseline, treatment days 1 through 5 and 1-week follow-up
Change from baseline in prespecified resting-state and LIFU-associated EEG measures of neural activity and functional connectivity.
Baseline, treatment days 1 through 5 and 1-week follow-up
To evaluate whether baseline fMRI feature predict clinical response to LIFU.
Tidsramme: Baseline, 1-week follow up and 4-week follow up visits
Associations between baseline fMRI features and absolute change from baseline in MADRS total score.
Baseline, 1-week follow up and 4-week follow up visits
To evaluate whether baseline EEG features predict clinical response to LIFU.
Tidsramme: Baseline, 1-week follow up and 4-week follow up visits
Associations between baseline EEG features and absolute change from baseline in MADRS total score.
Baseline, 1-week follow up and 4-week follow up visits

Samarbeidspartnere og etterforskere

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

Samarbeidspartnere

Etterforskere

  • Hovedetterforsker: Mahendra Bhati, MD, Stanford University

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. november 2026

Primær fullføring (Antatt)

31. desember 2028

Studiet fullført (Antatt)

31. desember 2028

Datoer for studieregistrering

Først innsendt

14. september 2026

Først innsendt som oppfylte QC-kriteriene

14. september 2026

Først lagt ut (Faktiske)

18. september 2026

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

18. september 2026

Siste oppdatering sendt inn som oppfylte QC-kriteriene

14. september 2026

Sist bekreftet

1. september 2026

Mer informasjon

Begreper knyttet til denne studien

Ytterligere relevante MeSH-vilkår

Andre studie-ID-numre

  • 85834 (Hillman)

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

Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .

Abonnere