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Low Field Magnetic Stimulation (LFMS) in Subjects With Treatment-Resistant Depression (TRD)

Depression Clinical Trial

Official title:
A Phase 2 Multicenter, Double-Blind, Placebo-Controlled, Dose Optimization Study of Low Field Magnetic Stimulation (LFMS) in Subjects With Treatment-Resistant Depression (TRD)

Clinical Trial Summary

The purpose of this study is to compare the relative effectiveness of 20 and 60 minutes of Low-Field Magnetic Stimulation in relieving symptoms in patients with major depression who are treatment resistant.

Clinical Trial Description

The primary objective of this study:

- To compare the relative efficacy, as measured by a change in the 6-item Hamilton Rating Scale for Depression (HAM-D6), of 20 and 60 minutes of LFMS compared to sham (placebo) in subjects with treatment resistant depression (TRD).

Secondary objectives:

- To determine if subjects with TRD may respond to 120 minutes of LFMS.

- To determine the persistence of response to LFMS therapy during the observation period.

- To evaluate the safety and tolerability of LFMS. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02452892
Study type Interventional
Source Tal Medical, Inc.
Contact
Status Completed
Phase N/A
Start date September 2015
Completion date October 2016
View Details
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