- ICH GCP
- Rejestr badań klinicznych w USA
- Badanie kliniczne 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.
Przegląd badań
Status
Szczegółowy opis
Typ studiów
Zapisy (Szacowany)
Faza
- Nie dotyczy
Kontakty i lokalizacje
Kontakt w sprawie studiów
- Nazwa: Masataka Wada, MD
- Numer telefonu: 650-434-7844
- E-mail: mwada@stanford.edu
Kopia zapasowa kontaktu do badania
- Nazwa: John P Coetzee, PhD
- E-mail: jpcoetzee@stanford.edu
Lokalizacje studiów
-
-
California
-
Stanford, California, Stany Zjednoczone, 94305
- Department of Psychiatry and Behavioral Sciences, Stanford School of Medicine
-
Kontakt:
- Nick Bassano, MSW
- Numer telefonu: 6504973933
- E-mail: nbassano@stanford.edu
-
Główny śledczy:
- Mahendra Bhati, MD
-
-
Kryteria uczestnictwa
Kryteria kwalifikacji
Wiek uprawniający do nauki
- Dorosły
Akceptuje zdrowych ochotników
Opis
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
Plan studiów
Jak projektuje się badanie?
Szczegóły projektu
- Główny cel: Leczenie
- Przydział: Randomizowane
- Model interwencyjny: Przydział równoległy
- Maskowanie: Podwójnie
Broń i interwencje
Grupa uczestników / Arm |
Interwencja / Leczenie |
|---|---|
|
Aktywny 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).
|
|
Pozorny 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).
|
Co mierzy badanie?
Podstawowe miary wyniku
Miara wyniku |
Opis środka |
Ramy czasowe |
|---|---|---|
|
To evaluate the safety and tolerability of repeated sgACC-targeted LIFU stimulation in adult Veterans with PTD.
Ramy czasowe: 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.
|
Miary wyników drugorzędnych
Miara wyniku |
Opis środka |
Ramy czasowe |
|---|---|---|
|
To evaluate the preliminary antidepressant efficacy of repeated sgACC-targeted LIFU in adult Veterans with PTD.
Ramy czasowe: 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
|
Inne miary wyników
Miara wyniku |
Opis środka |
Ramy czasowe |
|---|---|---|
|
To characterize changes in neuroimaging measures associated with LIFU.
Ramy czasowe: 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.
Ramy czasowe: 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.
Ramy czasowe: 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.
Ramy czasowe: 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
|
Współpracownicy i badacze
Sponsor
Współpracownicy
Śledczy
- Główny śledczy: Mahendra Bhati, MD, Stanford University
Daty zapisu na studia
Główne daty studiów
Rozpoczęcie studiów (Szacowany)
Zakończenie podstawowe (Szacowany)
Ukończenie studiów (Szacowany)
Daty rejestracji na studia
Pierwszy przesłany
Pierwszy przesłany, który spełnia kryteria kontroli jakości
Pierwszy wysłany (Rzeczywisty)
Aktualizacje rekordów badań
Ostatnia wysłana aktualizacja (Rzeczywisty)
Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości
Ostatnia weryfikacja
Więcej informacji
Terminy związane z tym badaniem
Słowa kluczowe
Dodatkowe istotne warunki MeSH
Inne numery identyfikacyjne badania
- 85834 (Hillman)
Informacje o lekach i urządzeniach, dokumenty badawcze
Bada produkt leczniczy regulowany przez amerykańską FDA
Bada produkt urządzenia regulowany przez amerykańską FDA
produkt wyprodukowany i wyeksportowany z USA
Te informacje zostały pobrane bezpośrednio ze strony internetowej clinicaltrials.gov bez żadnych zmian. Jeśli chcesz zmienić, usunąć lub zaktualizować dane swojego badania, skontaktuj się z register@clinicaltrials.gov. Gdy tylko zmiana zostanie wprowadzona na stronie clinicaltrials.gov, zostanie ona automatycznie zaktualizowana również na naszej stronie internetowej .