pBFS Guided VS "5-cm Rule" rTMS Over DLPFC for MDD

Status Recruiting

Clinical Trial Summary

The investigators aim to investigate whether the intervention effect of pBFS-guided rTMS therapy targeting DLPFC is superior to the intervention effect of the traditional "5 cm-rule" guided rTMS therapy in patients with depressive disorders.

Clinical Trial Description

After being informed about the study and potential risks. All patients giving written informed consent will undergo a screening period to determine eligibility for study entry. At week 0, patients who meet the eligibility requirements will be randomized in a blind manner in a 1:1 ratio to the pBFS group, or 5-cm rule group. Then all participants will undergo a 21-day rTMS modulation and 7-day, 14-day, and 45-day post-treatment follow-up visits. Participants will not take any other treatment during the intervention and the 7-day and 14-day post-treatment visits. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT05964023
Study type	Interventional
Source	Changping Laboratory
Contact	Meiling Li, Ph.D.
Phone	010-80726688
Email	meilingli@cpl.ac.cn
Status	Recruiting
Phase	N/A
Start date	August 20, 2023
Completion date	March 1, 2025

View Details

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