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

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

Completed

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Key information

Conditions

Bipolar Depression Bipolar Disorder Bipolar and Related Disorders Mental Disorders Mood Disorders

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

Shalvata MHC

Hod HaSharon, Israel

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Diagnosis of bipolar depression

Exclusion criteria

No other axis I disorder
Risk factors for convulsions

Treatment and study plan

H1 -coil TMS device

Device

Sponsors and collaborators

Lead sponsor

Shalvata Mental Health Center

Other

Registry information

Official study title

Evaluation of the H-Coil (TMS) Device - Safety and Feasibility in Bipolar Depression

Important dates

Study start: 2006
Study completion: 2008
First posted: Mar 8, 2007
Registry last updated: Feb 5, 2009

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.

Completed