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Deep Brain Stimulation for Treatment-Resistant Schizophrenia

2026년 9월 9일 업데이트: Johns Hopkins University

Deep Brain Stimulation in Treatment Resistant Schizophrenia

The purpose of this pilot study is to investigate the use of deep brain stimulation (DBS) of the substantia nigra pars reticulata (SNr) in subjects with treatment-resistant schizophrenia. There is a subset of patients with schizophrenia who continue to have persistent psychotic symptoms (auditory hallucinations and delusions) despite multiple adequate medication trials with antipsychotic medications including clozapine. There are currently no available treatments for such patients who generally have poor function and are chronically disabled, unable to work, live independently or have meaningful social relationships. Neuroimaging studies in patients with schizophrenia have revealed information about pathological neural circuits that could be suitable targets using deep brain stimulation. Although not yet tested in patients with schizophrenia, DBS is in early phase clinical trials in other psychiatric disorders.

This pilot study will investigate the use of DBS in treatment-resistant schizophrenia subjects who have exhausted all other therapeutic alternatives but continue to have persistent disabling psychotic symptoms. Of note, DBS is not FDA approved for use in patients with schizophrenia. The method will be similar to that used in subthalamic nucleus stimulation in patients with Parkinson's Disease. However, the electrode will be advanced slightly inferior into the SNr, a major outflow nucleus of the basal ganglia, with the intention of causing local inhibition of SNr outflow resulting in disinhibition of the mediodorsal nucleus (MDN) of the thalamus. Hypofunction of the MDN has been implicated in the pathophysiology of schizophrenia in post-mortem as well as multiple structural and functional imaging studies. Evidence suggests that dysfunction of the MD is implicated in both positive and cognitive symptoms (such as working memory impairment) in schizophrenia. Frequent monitoring and clinical assessment with psychiatric scales will be used to monitor treatment response.

연구 개요

연구 유형

중재적

등록 (추정된)

15

단계

  • 해당 없음

연락처 및 위치

이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.

연구 연락처

  • 이름: Nicola Cascella
  • 전화번호: (443)287-4195
  • 이메일: ncascel1@jhu.edu

연구 장소

    • Maryland
      • Baltimore, Maryland, 미국, 21287
        • The Johns Hopkins Hospital
        • 연락하다:

참여기준

연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.

자격 기준

공부할 수 있는 나이

  • 성인
  • 고령자

건강한 자원 봉사자를 받아들입니다

아니

설명

Inclusion Criteria:

  • Males and females who are at least 22 years of age.
  • Subject has a diagnosis of schizophrenia or schizoaffective disorder as determined by a review of medical records, discussion with referring psychiatrist as well as the Structured Clinical Interview for DSM-V (SCID-V).
  • Subject determined to be treatment-resistant for at least one year prior to the Screening Visit as demonstrated by clinical evidence (determined by review of medical records and discussion with referring psychiatrist) of persistent auditory hallucinations and/or delusions that have not responded to treatment with three adequate regimens of antipsychotic medication including one failed trial of clozapine as defined as follows:

    1. Adequate trials of two different antipsychotic drugs (not including clozapine) belonging to different classes of at least 12 weeks equivalent to at least 500 mg/day of chlorpromazine within the previous 5 years.
    2. A trial of clozapine of at least12 weeks at a dose of at least 400 mg (or a clozapine level of at least 350 ng/mL). Subjects who were unable to tolerate clozapine at this dose or for this duration because of intolerable side effects are also eligible.
  • Subject has at least a score of 6 (severe) on 2 of the 4 Brief Psychiatric Rating Scale (BPRS) positive symptoms (conceptual disorganization, grandiosity, hallucinatory behavior and unusual thought content) at all three Baseline Visits prior to undergoing surgery. One of the 2 must be hallucinatory behavior.
  • Subject must be ambulatory.
  • Females who are postmenopausal, physically incapable of childbearing, or practicing an acceptable method of birth control. Acceptable methods of birth control include surgical sterilization, hormonal contraceptives, or double-barrier methods (condom or diaphragm with a spermicidal agent or intrauterine device (IUD). If practicing an acceptable method of birth control, a negative urine pregnancy test result has been obtained at baseline Visits 1 and 3.
  • Subject is determined by independent psychiatrist with expertise in capacity assessments to have decision-making capacity to provide informed consent.
  • Subject is able to read English, understand and cooperate with study procedures, and has signed a written informed consent form prior to any study procedures.

Exclusion Criteria:

  • Subject has a positive urine drug screen at any of the three Baseline Visits.
  • Subject had major surgery within three months prior to Baseline Visit 1 or has other surgery planned during the proposed study period.
  • Subject is determined by medical consultant to have medical contraindications to undergoing surgery.
  • Subject is pregnant or breast-feeding.
  • Subject has a history of alcohol or drug abuse within the past 6 months and dependence within the past year.
  • Subject has a medical illness/condition, co-morbid psychiatric illness, and/or abnormal diagnostic finding that would interfere with the completion of the study, confound the results of the study, or pose risk to the patient.
  • Subject has participated in another investigational drug trial or therapeutic trial within 30 days of Baseline Visit 1.
  • Subject has a diagnosis of mental retardation.
  • Subject has a neurological condition, or a history of traumatic brain injury associated with loss of consciousness of > 1 hour and/or intracranial/epidural/subdural bleeding.
  • Subject has defibrillator or pacemaker or other implants that will interfere with MRI and functioning of the device.
  • Unstable psycho-social condition including housing and poor support.

공부 계획

이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.

연구는 어떻게 설계됩니까?

디자인 세부사항

  • 주 목적: 치료
  • 할당: 해당 없음
  • 중재 모델: 단일 그룹 할당
  • 마스킹: 없음(오픈 라벨)

무기와 개입

참가자 그룹 / 팔
개입 / 치료
실험적: 뇌심부자극 임플란트
비맹검 치료군, 치료 저항성 정신분열증에 대한 흑색질 ​​망상의 심부 뇌 자극.
치료 저항성 정신분열증의 만성 청각 환각 치료를 위한 심부 뇌 자극 시스템 배치

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
측정값 설명
기간
Change from baseline in the Brief Psychiatric Rating Scale
기간: 1 year after neurostimulator implantation
Investigators will assess deep brain stimulation effects on the positive and psychosis features of schizophrenia. Total scores range from 18 to 126. A higher score indicates a more severe psychiatric symptom rating.
1 year after neurostimulator implantation
Change from baseline in the Scales for the Assessment of Negative Symptoms (SANS)
기간: 1 year after neurostimulator implantation
Investigators will assess deep brain stimulation effects on negative symptoms aspects of schizophrenia. Score range 0-85. Higher scores indicate more severe negative symptoms.
1 year after neurostimulator implantation
Incidence of adverse device effects (ADEs).
기간: 1 year after neurostimulator implantation
Investigators will assess the incidence of adverse device effects as defined by the Code of Federal Regulations (21 CFR 812.3)
1 year after neurostimulator implantation

2차 결과 측정

결과 측정
측정값 설명
기간
Change from baseline in the Young Mania scale (YMS)
기간: 1 year after neurostimulator implantation
Investigators will assess deep brain stimulation effects on mania as assessed by the YMS. Score range 0-60 with higher score indicating greater severity of manic symptoms.
1 year after neurostimulator implantation
Change from baseline in the Measurement and Treatment Research to Improve Cognition in Schizophrenia (MATRICS) cognitive test battery.
기간: 1 year after neurostimulator implantation
Investigators will assess deep brain stimulation effects on cognition as assessed by the MATRICS cognitive test battery. The range of T-scores is between 0 to 100 with a mean of 50 and standard deviation of 10. Higher scores indicate better overall cognitive functioning.
1 year after neurostimulator implantation

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

수사관

  • 수석 연구원: Nicola Cascella, Johns Hopkins University

연구 기록 날짜

이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.

연구 주요 날짜

연구 시작 (추정된)

2026년 10월 1일

기본 완료 (추정된)

2029년 5월 30일

연구 완료 (추정된)

2029년 6월 28일

연구 등록 날짜

최초 제출

2026년 5월 12일

QC 기준을 충족하는 최초 제출

2026년 5월 12일

처음 게시됨 (실제)

2026년 5월 18일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2026년 9월 10일

QC 기준을 충족하는 마지막 업데이트 제출

2026년 9월 9일

마지막으로 확인됨

2026년 9월 1일

추가 정보

이 연구와 관련된 용어

기타 연구 ID 번호

  • IRB00554073

약물 및 장치 정보, 연구 문서

미국 FDA 규제 의약품 연구

아니

미국 FDA 규제 기기 제품 연구

예

이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .

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