- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT07828483
Development of Low-Intensity Focused Ultrasound for Post Traumatic Brain Injury Depression
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:
- the safety, tolerability, and feasibility of MRI-guided LIFU.
- Evaluate preliminary antidepressant efficacy.
- Characterize target engagement using multimodal neuroimaging and electrophysiology.
- Identify imaging and electrophysiological biomarkers that predict treatment response.
- Generate preliminary effect size estimates to support future multicenter clinical trials.
Studieoversikt
Status
Intervensjon / Behandling
Detaljert beskrivelse
Studietype
Registrering (Antatt)
Fase
- Ikke aktuelt
Kontakter og plasseringer
Studiekontakt
- Navn: Masataka Wada, MD
- Telefonnummer: 650-434-7844
- E-post: mwada@stanford.edu
Studer Kontakt Backup
- Navn: John P Coetzee, PhD
- E-post: jpcoetzee@stanford.edu
Studiesteder
-
-
California
-
Stanford, California, Forente stater, 94305
- Department of Psychiatry and Behavioral Sciences, Stanford School of Medicine
-
Ta kontakt med:
- Nick Bassano, MSW
- Telefonnummer: 6504973933
- E-post: nbassano@stanford.edu
-
Hovedetterforsker:
- Mahendra Bhati, MD
-
-
Deltakelseskriterier
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
- Voksen
Tar imot friske frivillige
Beskrivelse
Inclusion Criteria:
- Adult Veteran, male or female, 22 to 55 years of age at the time of screening.
- 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.
- 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.
- The TBI must have occurred at least 3 months before the occurrence of depression
- Current depressive disorder defined in the Diagnosis and Statistical Manual of Mental Disorders, Fifth Edition, Text Revision (DSM-5).
- 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).
- MADRS score of ≥20 at screening.
- Total duration of current depressive episode is less than 2 years
- LIFU naive.
- Access to ongoing psychiatric care before and after completion of the study.
- 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.
- In good general health, as evidenced by medical history.
- 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.
- Agreement to adhere to Lifestyle Considerations (see section 5.3) throughout study duration.
Exclusion Criteria:
- 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.
- Pregnancy
- Primary psychiatric condition other than MDD requiring treatment except stable comorbid anxiety disorder
- History of or current psychotic disorder or bipolar disorder
- Severe borderline personality disorder.
- Diagnosis of Intellectual Disability or Autism Spectrum Disorder
- Current moderate or severe substance use disorder or demonstrating signs of acute substance withdrawal
- Urine screening test positive for illicit substances
- Active suicidal ideation (defined as an MSSI > 8) or a suicide attempt (as defined by the C-SSRS) within the past one year
- 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
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
Sponsor
Samarbeidspartnere
Etterforskere
- Hovedetterforsker: Mahendra Bhati, MD, Stanford University
Studierekorddatoer
Studer hoveddatoer
Studiestart (Antatt)
Primær fullføring (Antatt)
Studiet fullført (Antatt)
Datoer for studieregistrering
Først innsendt
Først innsendt som oppfylte QC-kriteriene
Først lagt ut (Faktiske)
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
Siste oppdatering sendt inn som oppfylte QC-kriteriene
Sist bekreftet
Mer informasjon
Begreper knyttet til denne studien
Nøkkelord
Ytterligere relevante MeSH-vilkår
Andre studie-ID-numre
- 85834 (Hillman)
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