Loading clinical trials...
Loading clinical trials...
The primary aim of the study is to find the combination of neuroimaging-related markers, demographics, and clinical characteristics that predict the response of patients with therapy-resistant depression to theta-burst rTMS treatment. The secondary aim is to monitor the cognitive effects of TMS therapy.
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
No
Department of Psychiatry and Psychotherapy
Budapest, Pest County, Hungary
Start Date
June 13, 2025
Primary Completion Date
June 13, 2028
Completion Date
June 13, 2028
Last Updated
October 3, 2025
54
ESTIMATED participants
repetative Transcranial Magnetic Stimulation (rTMS), theta-burst protocol
DEVICE
Lead Sponsor
Semmelweis University
NCT06793397
NCT07422519
Data Source & Attribution
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.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and Conditions