Actively Recruiting

Phase Not Applicable
Age: 15Years +
All Genders
NCT07147218

Accelerated TMS for MDD

Led by Neuronetics · Updated on 2025-11-21

50

Participants Needed

3

Research Sites

123 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

An open-label, multi-center, prospective study to evaluate feasibility and efficacy of accelerated TMS for patients with Major Depressive Disorder (MDD).

CONDITIONS

Official Title

Accelerated TMS for MDD

Who Can Participate

Age: 15Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Male or female
  • 15 years and older
  • Able to provide informed consent or assent
  • Diagnosed with major depressive disorder (MDD) and currently experiencing a major depressive episode (MDE)
  • Adults must have failed to respond to at least one prior antidepressant medication; adolescents may use TMS as adjunct treatment without prior failure
  • Prescribed TMS therapy for MDD by their physician independent of study participation
  • On a stable antidepressant treatment regimen for at least 4 weeks and agree to maintain it during the study
  • Willing to comply with all study procedures, assessments, and visits, and available for study duration
Not Eligible

You will not qualify if you...

  • Contraindications for TMS per current treatment guidelines
  • MADRS score below 20 or PHQ score below 10 at screening or baseline
  • Current diagnosis of substance use disorder except nicotine dependence
  • Symptoms of substance withdrawal
  • History of schizophrenia, schizoaffective disorders, or psychotic symptoms in current or previous depressive episodes
  • Any disorder clinically predominant over MDD at screening or within 6 months prior
  • Clinically significant abnormality at screening affecting safety or study participation
  • Participation in any clinical trial with investigational drug or device within past month or concurrent
  • History of non-response to TMS or electroconvulsive therapy (ECT)
  • History of implanted device or psychosurgery for depression
  • Considered at significant risk for suicide by investigator
  • Any medical or psychological condition that would prevent study completion or affect data integrity

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 3 locations

1

Brighter Neurotherapeutics

New York, New York, United States, 10010

Actively Recruiting

2

TMS of the Carolinas

Charlotte, North Carolina, United States, 28210

Actively Recruiting

3

New chapter TMS

Spokane, Washington, United States, 99202

Actively Recruiting

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Research Team

N

Neha Goyal

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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