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NCT04106466 · ClinicalTrials.gov registry record · NA

DBS for TRD With the Medtronic Summit RC+S

A NA study of Major Depressive Disorder and Treatment-Resistant Depression, sponsored by Helen Mayberg, MD.

Active
Registry status
NA
Development phase
10
Enrollment target
1
Study location

NCT04106466: Active NA study of Major Depressive Disorder and Treatment-Resistant Depression, sponsored by Helen Mayberg, MD.

NCT04106466 is a NA study of Major Depressive Disorder and Treatment-Resistant Depression that is active but no longer recruiting, run by Helen Mayberg, MD. The registered enrollment target is 10 participants, below the 377-participant average among 282 other Major Depressive Disorder trials with a reported enrollment target (97% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT04106466, a NA study of Major Depressive Disorder and Treatment-Resistant Depression, is active but no longer recruiting, sponsored by Helen Mayberg, MD.

ACTIVE NOT RECRUITING
Registry status
NA
Development phase
10 participants
Enrollment target
1
Study location

Study Summary

Of the estimated 30 million Americans who suffer from Major Depressive Disorder, approximately 10% are considered treatment resistant. Deep brain stimulation (DBS) to a region of the brain called the subcallosal cingulate (SCC) is an emerging strategy for treatment resistant depression (TRD), which involves placement of electrodes in a specific region of the brain and stimulating that area with electricity. This is believed to reset the brain network responsible for symptoms and results in a significant antidepressant response. A series of open-label studies have demonstrated sustained, long-term antidepressant effects in 40-60% of patients who received this treatment. A challenge to the effective dissemination of this fledgling treatment is the absence of biomarkers (objective, measureable indications of the state of the body and brain) to guide device placement and select stimulation parameters during follow-up care. By using an experimental prototype DBS device called the Summit RC+S (Medtronic, Inc) which has the ability to both deliver stimulation to and record electrical signals directly from the brain, this study aims to identify changes in local field potentials (LFPs), specific electrical signals that are thought to represent how the brain communicates information from one region to another, to see how this relates to DBS parameter settings and patient depressive symptomatology. The goal of this study is to study LFPs before and during active DBS stimulation to identify changes that correlate with the antidepressant effects of SCC DBS. The study team will recruit 10 patients with TRD and implant them with the Summit RC+S system. Participants will be asked to complete short questionnaires and collect LFP data twice daily for the first year of the study, as well as have weekly in person research procedures and assessments with the study team for up to one year. These include meetings with the study psychiatrist, psychologist, symptom ratings, and periodic E

Primary Outcome

Change in Hamilton Depression Rating Scale (HDRS) score at 6 months and 1 year of continuous active stimulation as compared to preoperative baseline. The score for Hamilton Depression Rating Scale, 17 item version, full range from 0-50, with a higher score indicating more severe depression.

Interventions

  • DEVICE Medtronic Summit RC+S DBS system

Study Locations (1)

New York

  • Icahn School of Medicine at Mount Sinai, Mount Sinai West - New York

Trial Details

FieldValue
Enrollment Target 10 participants
Start Date 2020-01-21
Est. Completion 2030-12-31
Phase NA
Helen Mayberg, MD

2 total trials

What the registry record for NCT04106466 still lists

NCT04106466 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 10 participants, a relatively small participant target, below the 377-participant average among 282 other Major Depressive Disorder trials with a reported enrollment target (97% lower).

The record links to 2 conditions, with Major Depressive Disorder appearing as the primary indexed condition, and to 1 intervention - of which Medtronic Summit RC+S DBS system is the first listed.

NCT04106466 reports a single indexed study location in New York.

Frequently Asked Questions

What is clinical trial NCT04106466 about?

NCT04106466 is a clinical study titled "DBS for TRD With the Medtronic Summit RC+S". Of the estimated 30 million Americans who suffer from Major Depressive Disorder, approximately 10% are considered treatment resistant. Deep brain stimulation (DBS) to a region of the brain called the subcallosal cingulate (SCC) is an emerging strategy for treatment resistant depression (TRD), which ...

What is the current status of trial NCT04106466?

This trial is currently active not recruiting. It is a NA study. The enrollment target is 10 participants. The study started on 2020-01-21. Estimated completion is 2030-12-31.

What conditions does trial NCT04106466 study?

This clinical trial studies the following conditions: Major Depressive Disorder, Treatment-Resistant Depression.

What interventions are being tested in trial NCT04106466?

The interventions under investigation include: Medtronic Summit RC+S DBS system (DEVICE).

Who is sponsoring clinical trial NCT04106466?

This trial is sponsored by Helen Mayberg, MD, which has 2 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT04106466 being conducted?

This trial has 1 study location across New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Major Depressive Disorder

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT04106466's enrollment target sits among peer trials

10 272nd of 282 higher than 5 of 282 other Major Depressive Disorder trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Major Depressive Disorder trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT04106466, the US trial registry maintained by the National Library of Medicine. NCT04106466 (small enrollment · single site footprint · active not recruiting) retrieved and formatted by PlainTrial, see methodology.