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Clinical Trial Summary

The primary objective of this study is to determine the safety and efficacy of ultrasound as a treatment for Obsessive Compulsive disorder.


Clinical Trial Description

The present study is being undertaken as an open-label study to evaluate the safety and feasibility of focused ultrasound as an intervention for patients with obsessive compulsive disorder (OCD). Participants in this study will undergo 8 consecutive weekly sessions of transcranial low-intensity focused ultrasound (LIFUP) targeting the caudate of the basal ganglia. The safety of this protocol will be closely monitored and data will be used to determine whether any significant safety issues exist when using focused ultrasound for this neurological application. Treatment response will be measured using the Beck Depression & Anxiety Inventories, the Yale-Brown Obsessive-Compulsive Scale, and the Global Rating of Change Scale. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04775875
Study type Interventional
Source Neurological Associates of West Los Angeles
Contact
Status Enrolling by invitation
Phase N/A
Start date December 1, 2020
Completion date December 31, 2025

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