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Clinical Trial Summary

We are investigating the feasibility and efficacy of transcranial magnetic stimulation (TMS) for patients with GAD who were placebo nonresponders in DIEF003523.1.


Clinical Trial Description

Approximately five patients with GAD who failed to respond to a sham (placebo) TMS intervention will be enrolled. TMS sessions will occur twice a week for five weeks. Assessments will occur at pretreatment, weekly during treatment, and at posttreatment. Approximately five nonanxious control volunteers will also be recruited to complete pretreatment assessments for baseline comparison purposes. ;


Study Design

Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT01815099
Study type Interventional
Source Hartford Hospital
Contact Gretchen J Diefenbach, Ph.D.
Phone 860-545-7396
Email gretchen.diefenbach@hhchealth.org
Status Recruiting
Phase N/A
Start date May 2014
Completion date May 2015

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