Accelerated TMS for Treatment-Resistant ECT

Recruiting now · Not applicable

Conditions studied: Major Depressive Disorder (MDD)

In brief

This study investigates whether an additional treatment using transcranial magnetic stimulation (TMS) can help severely depressed patients who did not respond well to electroconvulsive therapy (ECT). All participants will first receive standard ECT treatment for depression, including brain scans (fMRI), psychological testing, clinical assessments, and the collection of blood and stool samples. If the ECT treatment is not effective, patients will be invited to participate in a second part of the study where they receive a 4-day course of accelerated TMS (20 sessions in total). The study aims to assess whether this additional TMS treatment can reduce depressive symptoms. The study also explores how brain structure, genetics, and gut health may relate to treatment success. In total, 200 patients will be included.

Key facts

Study ID

NCT07115628

Run by

Universitair Ziekenhuis Brussel

People needed

200

Starts

2025-10-01

Expected to finish

2028-12-01

Last updated by the study team

2025-08-11

Who can join

Age: 18 and older, up to 70. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Diagnosis of Major Depressive Disorder (MDD)
• Age between 18 - 70 years
• Referred for ECT treatment

You may not qualify if…

• A personal history of seizures or epilepsy, a history of seizures or epilepsy in first degree relatives and the presence of any known factor that can lower the seizure threshold (sleep deprivation, abuse substance, etc.), previous head injury and the presence of metallic implants in the cephalic region (e.g., aneurysm clips, shunts, stimulators, cochlear implants, electrodes) except dental fill-ings and the presence of cardiac pacemakers, neurostimulators, surgical clips or other electronic equipment, comorbidity with some neurological disorders: increased intracranial pressure, space-occupying lesion, history of stroke or transient ischemic attack, brain aneurysm and any structural brain damage with increased risk for epilepsy detected with MRI
• Patients with cognitive disturbances or dementia (Mini Mental State) < 24
• Suicide attempt within 6 months before the start of the study or pre-sent risk of suicide per the investigator's clinical judgment

Where it is running

• UZ Brussel — Jette, Brussels Capital, Belgium (enrolling)

Full record on ClinicalTrials.gov

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