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Tractography Guided Subcallosal Cingulate Deep Brain Stimulation for Treatment Resistant Depression

Launched by NADER POURATIAN · May 14, 2019

Trial Information

Current as of July 04, 2025

Recruiting

Keywords

ClinConnect Summary

This clinical trial is investigating a new approach to deep brain stimulation (DBS) surgery for people with treatment-resistant depression. Treatment-resistant depression is when a person has not found relief from their depression despite trying multiple treatments. The researchers will use advanced imaging techniques to help identify the best areas of the brain to target during surgery. This study aims to see if this method is safe and effective in improving mood in participants.

To be eligible for the trial, participants need to be between 21 and 70 years old, have been diagnosed with major depressive disorder for at least two years, and have tried at least four different depression treatments without success. Additionally, they should have a stable medication regimen for at least 30 days before the study. Participants can expect to undergo brain imaging and regular check-ups for at least a year, during which their mood will be monitored to see how well the surgery works. It's important to note that some individuals may not qualify if they have certain mental health conditions, a history of substance abuse, or other medical issues that could complicate surgery.

Gender

ALL

Eligibility criteria

  • 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.

About Nader Pouratian

Nader Pouratian is a distinguished clinical trial sponsor with a focus on advancing innovative therapeutic solutions in the field of neurology and pain management. With a robust background in clinical research and a commitment to improving patient outcomes, Pouratian leads initiatives that bridge scientific discovery and practical application. His work emphasizes the importance of rigorous study design, ethical standards, and collaborative partnerships, aiming to translate cutting-edge research into viable treatment options for patients. Through his leadership, clinical trials under his sponsorship are characterized by their integrity, scientific excellence, and dedication to enhancing quality of life for individuals affected by neurological disorders.

Locations

Dallas, Texas, United States

Patients applied

0 patients applied

Trial Officials

Nader Pouratian, MD, PhD

Principal Investigator

UT Southwestern Medical Center

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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