Viewing Study NCT03240692



Ignite Creation Date: 2024-05-06 @ 10:23 AM
Last Modification Date: 2024-10-26 @ 12:29 PM
Study NCT ID: NCT03240692
Status: COMPLETED
Last Update Posted: 2022-04-21
First Post: 2016-04-23

Brief Title: Stanford Accelerated Intelligent Neuromodulation Therapy for Treatment-Resistant Depression OL Cohort
Sponsor: Stanford University
Organization: Stanford University

Study Overview

Official Title: Stanford Accelerated Intelligent Neuromodulation Therapy for Treatment-Resistant Depression SAINT-TRD
Status: COMPLETED
Status Verified Date: 2022-04
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: SAINT-TRD
Brief Summary: This study evaluates an accelerated schedule of theta-burst stimulation using a transcranial magnetic stimulation device for treatment-resistant depression In this open label study all participants will receive accelerated theta-burst stimulation
Detailed Description: Repetitive transcranial magnetic stimulation rTMS is an established technology as therapy for treatment-resistant depression The approved method for treatment is 10Hz stimulation for 40 minutes over the left dorsolateral prefrontal cortex L-DLPFC for a 6 week treatment course This methodology has been successful for many people with treatment-resistant depression One of the limitations of this approach is the long duration of the treatment course approximately a 6 weeks per treatment course Recently researchers have aggressively pursued modifying the treatment parameters to reduce treatment course time with some preliminary success This study intends to further modify the parameters to create a more rapid form of the treatment This study will also look at the change in neuroimaging biomarkers associated with this treatment

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: True
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: False
Is an FDA AA801 Violation?: None