Evaluation of the H-Coil Transcranial Magnetic Stimulation (TMS) Device in the Treatment of Bipolar Depression

NCT ID: NCT00444938

Last Updated: 2009-02-05

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

COMPLETED

Clinical Phase

PHASE1

Study Classification

INTERVENTIONAL

Study Start Date

2006-06-30

Study Completion Date

2008-03-31

Brief Summary

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This study is evaluating the potential antidepressive effect of a 4 week treatment protocol using the H-coil deep TMS device in bipolar depression.

Detailed Description

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Conditions

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Bipolar Depression

Study Design

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Allocation Method

NON_RANDOMIZED

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Interventions

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H1 -coil TMS device

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

* Diagnosis of bipolar depression

Exclusion Criteria

* No other axis I disorder
* Risk factors for convulsions
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Shalvata Mental Health Center

OTHER

Sponsor Role lead

Principal Investigators

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Eiran V Harel, MD

Role: PRINCIPAL_INVESTIGATOR

Shalvata MHC

Locations

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Shalvata MHC

Hod HaSharon, , Israel

Site Status

Countries

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Israel

References

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Harel EV, Zangen A, Roth Y, Reti I, Braw Y, Levkovitz Y. H-coil repetitive transcranial magnetic stimulation for the treatment of bipolar depression: an add-on, safety and feasibility study. World J Biol Psychiatry. 2011 Mar;12(2):119-26. doi: 10.3109/15622975.2010.510893. Epub 2010 Sep 21.

Reference Type DERIVED
PMID: 20854181 (View on PubMed)

Other Identifiers

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SH-50506

Identifier Type: -

Identifier Source: org_study_id

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