Brain zaps guided by scans: a new hope for untreatable depression?
NCT ID NCT03952962
First seen Jul 15, 2026 · Last updated Jul 16, 2026 · Updated 1 time
Summary
This study tests a new way to perform deep brain stimulation (DBS) for people with severe depression that hasn't improved with standard treatments. Instead of targeting a fixed brain region, the researchers use advanced MRI scans to tailor the stimulation to each person's brain network. The goal is to see if this personalized approach is safe and can reduce depression symptoms.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- deep brain stimulation using the Abbott Laboratories Infinity™ implantable system
- What this could lead to
- If successful, this approach could offer a more precise and effective way to treat severe depression that hasn't responded to other therapies.
- What could go wrong
- This is a small, early feasibility study, so results may not apply broadly. Deep brain stimulation carries surgical risks and may not work for everyone.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 12 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Oct 2022
- Expected to finish
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Jul 2027
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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21 to 70 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Men and women (non-pregnant) between ages 21 and 70; * DSM-5 diagnosis a current major depressive episode (MDE) for 10 years of less, recurrent or single episode with first episode after adulthood and did not start during childhood or adolescence, secondary to nonpsychotic unipolar major depressive disorder; * Current index MDE ≥24 months duration and/or recurrent illness with at least a total of 2 lifetime episodes (including current episode \>12 months); * Treatment resistance (defined by criteria on the Antidepressant Treatment History Form (ATHF)28): Failure to respond to a minimum of four adequate depression treatments from different categories; * Symptom severity for Screening: Hamilton Depression Rating Scale-17 item (HDRS17) ≥20; * Symptom severity for Outcome: Montgomery Asberg Rating Scale (MADRS) ≥27 to be met at assessment one week pre-op; * Normal brain MRI within 3 months of surgery; * Antidepressant medication regimen has been held stable for ≥ 30 days prior to the study screening MADRS; * Remain on stable antidepressant medication throughout the study, unless there are safety concerns; * Montreal Cognitive Assessment (MoCA) \>25; * Able and willing to give informed consent and agree to attend regular clinic visits for at least 12 months. Exclusion Criteria: * DSM-5 Axis I Disorders: any lifetime history of psychotic disorder or bipolar disorder; * Alcohol or substance use disorder within 6 months, excluding nicotine; * History of childhood abuse (physical or sexual) 18 * Personality disorders; * Seeking disability during the trial; * Current substantial suicidal risk as defined by a plan or clear immediate intent for self-harm, or made any suicide attempt within the last year; (MADRS ≥ 5 including the day of surgery); * No stable work history; * Neurological/Medical condition that makes the patient, in the opinion of the surgeon, a poor candidate; 1. Pregnant or has plans to become pregnant in the next 36 months; 2. Unable/unable to practice birth control through the period of randomization and withdrawal of therapy; * Subjects who have a history of a seizure disorder; * Subjects who will be exposed to diathermy; * Subjects who have any medical contraindications to undergoing DBS surgery (e.g. infection, coagulopathy, or significant cardiac or other medical risk factors for surgery); * Subjects with another implanted device such as a cardiac pacemaker, defibrillator or neurostimulator; * Subjects who have a history of hemorrhagic stroke; * Subjects who are unable to undergo MRI; * Subjects who are at increased risk of hemorrhage due to underlying medical conditions or medication.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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UT Southwestern Medical Center
RECRUITINGDallas, Texas, 75390, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Biotype-assigned augmentation approach in resistant Late-Life depression (BAARD): a randomized controlled trial
- Neural and antidepressant effects of propofol
- Can pairing ketamine with talk therapy beat depression alone?
- Can a psychedelic drug lift depression that won't budge?
- Can a 6,000-Person study unlock personalized depression care for asians?
- A Brain-Stimulation showdown: can accelerated therapy outpace standard care for depression?