NCT07684794尚未招募不适用
Regulated Stimulation for Optimized Network Activity and Therapeutic Equilibrium - Maintenance
Motif Neurotech, Inc.0 个研究点目标入组 10 人开始时间: 2026年8月10日最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 发起方
- 入组人数
- 10
- 主要终点
- Incidence of device and/or procedure-related adverse events (AEs)
研究概览
简要总结
The objective of this study is to evaluate the safety, tolerability, and preliminary efficacy of the Motif XCS System when used as indicated for treatment-resistant depression (TRD).
详细描述
The Motif XCS System study is a prospective, multi-center, single-arm, open-label early feasibility study (EFS).
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 22 Years 至 85 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Has a diagnosis of unipolar non-psychotic Major Depressive Disorder (MDD) and is currently experiencing a major depressive episode (MDE) as defined by DSM-5
- •Has a screening Montgomery-Åsberg Depression Rating Scale (MADRS) score of ≥20
- •Has not had a sustained response to 2 or more adequately dosed antidepressant treatments from at least 2 different antidepressant treatment classes in at least one episode of major depressive disorder, according to the Antidepressant Treatment History Form (ATHF)
- •Is willing and able to provide written informed consent
- •Is 22-85 years of age
- •Is willing and able to comply with the protocol, including follow-up visits
- •Has been on a stable psychiatric treatment regimen for 30 days before the study screening MADRS and is willing to maintain a stable psychiatric treatment regimen through the Week 4 follow-up visit
排除标准
- •Has a cranial implant (with the exception of dental implants), neurostimulator, implanted medication pump, spinal cord stimulator, or pacemaker/implantable cardioverter-defibrillator
- •Has knowledge of planned magnetic resonance imaging (MRIs) in the next 12 months, after implant
- •Is unable to undergo imaging with computed tomography (CT), magnetic resonance imaging (MRI), diffusion tensor imaging (DTI), or functional magnetic resonance imaging (fMRI)
- •In the opinion of the investigator, the implant and therapy pose an unacceptable surgical or medical risk to the patient
- •Is currently taking blood thinners and cannot be taken off blood thinners
- •Has taken ketamine or esketamine in the past 30 days or is planning on taking ketamine or esketamine before the 4-week follow-up visit
- •Has taken hallucinogenic or dissociative medications in the past 30 days or is planning on taking hallucinogenic or dissociative medications for the treatment of mood or anxiety disorders before the 4-week follow-up visit
- •Has a history of bipolar disorder
- •Has a history of schizophrenia, schizoaffective disorder, or other psychotic disorder
- •Has psychotic features in the current depressive episode
- •Has a chronic and clinically significant neurological disorder (epilepsy, dementia, delirium, amnestic disorder, brain tumor), or neuroimaging findings that would potentially impact the efficacy of treatment (e.g., extensive white matter disease, demyelinating lesions, atrophy, brain tumor)
- •Currently taking medication that would alter the seizure threshold, increasing potential seizure risks
- •Has a history of brain injury that resulted in current cognitive impairment
- •Has a history of bony disorders that impact the safe and effective use of the device as well as device implantation
- •Has a history of skin disorders that impact the safe and effective use of the device as well as device implantation
- •Has failed all attempts to achieve at least 50% reduction in depressive symptoms after completion of approved treatment courses of electroconvulsive therapy (ECT) or TMS for treatment of MDD
- •Is planning to receive any other neuromodulation therapy (e.g., ECT, TMS, tDCS, tACS, DBS, VNS, or focused ultrasound) during the study
- •Meets the DSM-5 criteria for alcohol use disorder or other substance use disorder (not including tobacco/nicotine) within 12 months prior to study enrollment or, in the opinion of the investigator, is using illicit drugs recreationally or therapeutically which could impact the safety or effectiveness of the therapy
- •Female who is pregnant at the time of inclusion, or planning to become pregnant during the duration of the study, or not willing to use an effective method of birth control
- •Has a life expectancy less than 12 months
- •In the opinion of the investigator, is considered to be acutely suicidal (e.g., Type 4 or 5 on the C-SSRS)
- •In the investigator's opinion, any known comorbidity that would complicate the assessment of safety or prevent participation in follow-up visits
- •Before implantation of the Motif DOT Implant, subjects must continue to meet all study eligibility criteria. Subjects must also meet the following additional criteria:
- •Psychiatric treatment regimen has remained stable
- •Has skull thickness ≥5.5 mm and ≤15.5 mm over the implant target
结局指标
主要结局
Incidence of device and/or procedure-related adverse events (AEs)
时间窗: During procedure to 12 months follow-up
次要结局
- Change in score on clinical outcome measures of treatment-resistant depression (Montgomery-Åsberg Depression Rating Scale [MADRS])(After treatment to 12 months follow-up)
- The incidence of stimulation-induced side effects(After treatment to 12 months follow-up)
研究者
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