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COMPLETED NA

TMS for Suicidal Crisis in Active Duty SMs

NCT03014362 · View on ClinicalTrials.gov ↗

Study Summary

The purpose of this study is to determine if the use of Transcranial Magnetic Stimulation (TMS) provides rapid reduction and sustained attenuation of suicidal crisis. TMS is a treatment for suicidal crisis that is quicker, less invasive, better tolerated, and with fewer side effects than current treatments such as Electroconvulsive Therapy (ECT) and medication therapies. There will be 6 months of follow-up, in order to establish the ongoing and lasting therapeutic effect of TMS.

Interventions

  • DEVICE Neuronetics NeuroStar XPLOR magnetic stimulator - Active
  • DEVICE Neuronetics NeuroStar XPLOR magnetic stimulator - Sham

Study Locations (1)

Georgia

  • Eisenhower Army Medical Center — Augusta

Trial Details

FieldValue
Enrollment Target 120 participants
Start Date 2017-06-12
Est. Completion 2021-09-10
Phase NA

Sponsor

Eisenhower Army Medical Center

2 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT03014362

The ClinicalTrials.gov registry entry for NCT03014362 describes a study currently listed as completed. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 120 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Eisenhower Army Medical Center, which has 2 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 6 conditions, with Suicide appearing as the primary indexed condition, and to 2 interventions — of which Neuronetics NeuroStar XPLOR magnetic stimulator - Active is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT03014362 reports 1 study location spanning 1 distinct geographic area — top geographies include Georgia. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT03014362 about?

NCT03014362 is a clinical study titled "TMS for Suicidal Crisis in Active Duty SMs". The purpose of this study is to determine if the use of Transcranial Magnetic Stimulation (TMS) provides rapid reduction and sustained attenuation of suicidal crisis. TMS is a treatment for suicidal crisis that is quicker, less invasive, better tolerated, and with fewer side effects than current tre...

What is the current status of trial NCT03014362?

This trial is currently completed. It is a NA study. The enrollment target is 120 participants. The study started on 2017-06-12. Estimated completion is 2021-09-10.

What conditions does trial NCT03014362 study?

This clinical trial studies the following conditions: Suicide, Suicidal Ideation, Suicidal Intention, Suicidal Impulses, Suicidal and Self-Injurious Behavior. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT03014362?

The interventions under investigation include: Neuronetics NeuroStar XPLOR magnetic stimulator - Active (DEVICE), Neuronetics NeuroStar XPLOR magnetic stimulator - Sham (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT03014362?

This trial is sponsored by Eisenhower Army Medical Center, which has 2 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT03014362 being conducted?

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

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial