Can a blood test predict who benefits from magnetic brain stimulation?
NCT ID NCT07039370
First seen Sep 11, 2026 · Last updated Sep 11, 2026
Summary
Researchers are studying whether blood proteins and metabolites can predict who responds to transcranial magnetic stimulation (TMS) for treatment-resistant depression. About 55 adults whose depression has not improved with at least two antidepressants receive 20 sessions of intermittent theta burst stimulation, a form of TMS. The team measures protein and metabolite levels in blood before and after treatment and compares responders with non-responders. The goal is to find biological signatures that could guide more personalized treatment choices.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Transcranial magnetic stimulation (TMS), a non-invasive brain stimulation technique
- What this could lead to
- If researchers can link blood markers to TMS response, doctors may one day pick the right treatment for each person faster and avoid months of trial and error.
- What could go wrong
- This is a small study of 55 people at a single hospital, so any marker it flags may not hold up in larger, more diverse groups. Blood protein and metabolite levels shift for many reasons, which makes clear signals hard to isolate.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
-
About 55 people
The number the study aims to enrol. It can still change while the study runs.
- Started
-
Jun 2025
- Expected to finish
-
Jun 2027
An estimate. End dates often move.
- Lead sponsor
-
A government agency
The lead sponsor is a government body.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
18 to 65 years
- Sex
-
Anyone
- Healthy volunteers
-
Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Diagnosis of Major Depressive Disorder (MDD) according to DSM-5-TR criteria. * Inadequate clinical response to at least two different antidepressants and/or anti-obsessive agents administered at therapeutic doses and durations. * Clinical symptoms not better explained by metabolic or organic medical conditions. * No epileptic activity detected on routine electroencephalography (EEG) prior to TMS initiation. * Routine pre-TMS laboratory tests reveal no abnormalities that may significantly affect treatment response, including: * Normal thyroid hormone profile * No significant vitamin deficiencies * No markedly elevated inflammatory markers * No history or current evidence of hearing loss on clinical evaluation; if present, evaluation by an otolaryngologist will be obtained. * Age 18 years and older. * Ability to provide written informed consent. Exclusion Criteria: * Any contraindication to TMS as identified in the standardized pre-TMS risk assessment form. * Presence of epileptic focus detected on pre-TMS EEG. * History of significant head trauma, loss of consciousness, or intracranial surgery. * Presence of metal implants or foreign bodies incompatible with TMS (e.g., aneurysm clips, surgical clamps, metallic fragments). * Abnormal thyroid hormone levels in pre-TMS laboratory testing. * Significantly elevated inflammation markers (e.g., CRP) in pre-TMS bloodwork. * Vitamin deficiencies associated with cognitive impairment (e.g., B12, folate) in pre-TMS labs. * Electrolyte imbalances on pre-TMS blood testing. * History of psychotic disorder or bipolar I/II disorder. * History of substance-induced psychosis or bipolar disorder. * Current or past substance use disorder (including alcohol, stimulants, or illicit drugs), unless abstinent from substances (excluding alcohol) for a minimum of 12 months. * Voluntary discontinuation of TMS during the treatment course. * Any serious adverse event or unexpected clinical condition during treatment that necessitates discontinuation of TMS.
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for Major depression disorder are added.
By submitting, you agree to our Terms of use
Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
-
The places running it
2 sites. The list below names each one and where it is.
-
The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
-
A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
-
Gulhane Training and Research Hospital
RECRUITINGAnkara, Ankara, 06000, Turkey (Türkiye)
-
Gulhane Training and Research Hospital
RECRUITINGAnkara, Ankara, 06300, Turkey (Türkiye)
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Which ketamine works better for severe depression? a 5-Year study aims to find out
- Psychedelic DMT studied for depression relief in early human trial
- Could a light beam lift depression when drugs fail?
- Could a headset at home lift depression? new trial investigates
- Teens use phone app to stop anxiety and depression from coming back