Evaluation of the H-coil Transcranial Magnetic Stimulation TMS Device - Safety and Feasibility Study for Acute and Maintenance Treatment in Major Depressive Episode

Shalvata Mental Health Center

Status and phase: Completed; Phase 2

Conditions: Major Depressive Disorder

Treatments: Device: H-coil dTMS

Study type: Interventional

Funder types: Other; Industry

Identifiers

NCT00807105

0013-07 SHA

Details and patient eligibility

About

This is a prospective open label study of acute and maintenance treatment of MDD. The acute phase consists of daily treatments for 4 weeks. maintenance will be twice a week for eight weeks followed by 10 weeks of once a week treatments.

Enrollment: 29 patients

Sex: All

Ages: 18 to 65 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• MDD patients

Exclusion criteria

• risk factors for convulsions

Trial design

Primary purpose: Treatment

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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29 participants in 1 patient group

depressive patients

Experimental group

Description:

patients suffering from deppresion

Treatment:

Device: H-coil dTMS