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The primary objective of this study is to optimize the protocol for the TUS administration in patients with TRD while gaining an initial impression of treatment efficacy.
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Lead Sponsor
Centre Hospitalier St Anne
NCT07088380 · Major Depressive Disorder, Treatment Resistant Depression
NCT06938841 · Major Depressive Disorder, Treatment Resistant Depression
NCT06731621 · Treatment Resistant Depression, Autism Spectrum Disorder
NCT03537794 · Treatment Resistant Depression
NCT05905705 · Treatment Resistant Depression
GHU Sainte-Anne
Paris
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This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
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