Clinical Trials Logo

Clinical Trial Summary

Chronic intracalvarial cortical stimulation is a minimally invasive method involving the neurosurgical placement of an electrode above the inner table of the skull. Over time, intracalvarial cortical stimulation is intermittently activated to modulate locally and distally connected brain regions. Because of the important role played by the dorsolateral prefrontal cortex in mood regulation, the goal of this study is to apply intracalvarial prefrontal cortical stimulation (IpCS) over the dorsolateral prefrontal cortex in severely treatment-resistant depressed (TRD) patients. Per the DSM-V and Centre for Medicare and Medicaid Services (CMS) nomenclatures, TRD patients are commonly defined as those whose treatment failed to produce response or remission after 2 or more attempts of sufficient duration and treatment dose. In the investigator's study, eligible TRD subjects will have a diagnosis of major depressive disorder with a suboptimal response to an adequate dose and duration of at least two different antidepressant treatment categories. These subjects will also have had exposure and transiently (non-durably) responded to non-invasive neurostimulation. The investigator anticipates that severely Treatment Resistant Depressed (TRD) Subjects with IpCS of the dorsolateral prefrontal cortex will show a significant decrease in depression symptoms as measured by the Montgomery-Asberg Depression Rating Scale (MADRS) at four months post-implant when compared to baseline. The investigator will enroll up to 20 subjects with severe refractory depression in an open trial, followed for up to one year. Depressive and cognitive symptoms will be rated periodically to assess the safety and efficacy of this procedure.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05393622
Study type Interventional
Source Inner Cosmos Inc
Contact Arthur Gribetz
Phone +1 650 704 3202
Email arthur@innercosmos.io
Status Recruiting
Phase N/A
Start date July 28, 2022
Completion date December 2025

See also
  Status Clinical Trial Phase
Not yet recruiting NCT05539495 - Exercise Recovery From Persistent Depression: A Thematic Analysis
Completed NCT04266288 - Effectiveness of Ketamine for Depression and Suicidal Ideation in the Emergency Department Phase 4
Recruiting NCT04916626 - The OPUS YOUNG Trial. Early Intervention Versus Treatment as Usual for Adolescents With First-episode Psychosis N/A
Recruiting NCT06374056 - Kintsugi Voice Device Pilot Study
Completed NCT05686408 - Study to Evaluate TNX-601 ER Monotherapy Versus Placebo in Patients With Major Depressive Disorder (MDD) Phase 2
Recruiting NCT04211467 - A Non-Interventional Pilot Study to Explore the Role of Gut Flora in Depression
Recruiting NCT06273995 - Telehealth Behavioral Activation for Teens N/A
Terminated NCT04260607 - Initiating Ketamine in Acutely Suicidal Patients in the Emergency Department Phase 3
Recruiting NCT04404309 - Outcomes Associated With Suicidality in Inpatients With Symptoms of Depression (OASIS-D)
Recruiting NCT05788198 - Integrated Depression Care N/A