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Clinical Trials/NCT00018746
NCT00018746CompletedPhase 1

Efficacy of Threshold vs. Subthreshold TMS in the Treatment of Depression

US Department of Veterans Affairs1 site in 1 countryStarted: July 1, 1999Last updated:
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Conditions

Trial Snapshot

Phase
Phase 1
Status
Completed
Locations
1
Study OverviewStudy DesignEligibility CriteriaInvestigatorsSitesRecords & IdentifiersSimilar Trials

Study Overview

Brief Summary

The study examines efficacy of repetitive transcranial magnetic stimulation in treating severely depressed patients who are medicated.

Detailed Description

Medicated, treatment resistant, depressed patients are randomized to active or sham repetitive transcranial magnetic stimulation (rTMS). Responding patients go into a six months follow-up period.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Crossover
Primary Purpose
Treatment
Masking
Single

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •severe treatment-resistant depression

Exclusion Criteria

  • Not provided

Investigators

Sponsor Class
Fed

Study Sites (1)

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