Retrospective Analyses of TrakStar Database

NCT ID: NCT06917339

Last Updated: 2025-04-08

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Total Enrollment

156000 participants

Study Classification

OBSERVATIONAL

Study Start Date

2025-02-25

Study Completion Date

2035-12-31

Brief Summary

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In this study, real-world data will be used to better understand the effects patient characteristics, symptoms and TMS protocol parameters have on clinical outcomes with NeuroStar TMS.

Detailed Description

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Conditions

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Depression Obsessive-Compulsive Disorder Anxiety Depression

Study Design

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Observational Model Type

COHORT

Study Time Perspective

RETROSPECTIVE

Study Groups

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Patients treated with NeuroStar TMS

NeuroStar Advanced TMS Therapy System

Intervention Type DEVICE

non-invasive brain stimulation device

Interventions

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NeuroStar Advanced TMS Therapy System

non-invasive brain stimulation device

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

* Male or female reported in database and not an invalid entry
* Age reported and not an invalid entry
* Treatment date of November 01, 2008 or later.

Exclusion Criteria

• Incomplete information on treatment parameters
Minimum Eligible Age

5 Years

Maximum Eligible Age

120 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Neuronetics

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Eleanor Cole, PhD

Role: STUDY_DIRECTOR

Neuronetics

Locations

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Neuronetics

Malvern, Pennsylvania, United States

Site Status RECRUITING

Countries

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United States

Central Contacts

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Neha Goyal

Role: CONTACT

763-528-1599

Eleanor Cole, PhD

Role: CONTACT

415-724-7960

Facility Contacts

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Eleanor Cole

Role: primary

Other Identifiers

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11-10000-000

Identifier Type: -

Identifier Source: org_study_id

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