Review the details below, then apply to join this clinical trial.
At a Glance
Age
18 and older
Sex
Any
Trial phase
Early Phase 1
Study type
Interventional
Purpose
Basic Science
Participants needed
80 (estimated)
Sponsor
Mclean Hospital · Other
Who this trial is looking for
This trial is looking for people with major depression who have not improved with standard treatments. Participants will receive a specific type of brain stimulation along with a medication or placebo to see how it affects their brain activity.
Are You a Good Fit for This Trial?
You may be able to join if
I can safely receive TMS and study drugs
I have a stable medication regimen for one month prior to the study
I am not currently receiving TMS, ECT, or ketamine
I do not have active safety concerns related to suicidality
I have moderate to severe Major Depressive Disorder
You may not be able to join if
I have a history of seizures or epilepsy
I have a history of brain injuries
I have signs of increased pressure in my brain
I have any major neurological conditions
I have major medical conditions that may cause emergencies if I have a seizure
I have severe migraines that may make treatment difficult
I cannot tolerate an MRI
I am pregnant
Summarized in plain language from this trial's official eligibility criteria.
The full criteria are further down this page — only the research team can
confirm whether you qualify.
Think this trial could be right for you?
Answer three quick questions written from this study's own rules to see if you may qualify. No account needed to find out.
Many people with depression do not get better with standard treatments like medication. One promising alternative is transcranial magnetic stimulation (TMS), a non-invasive procedure that uses magnetic pulses to stimulate specific brain regions. A particular pattern of TMS called continuous theta-burst stimulation (cTBS) is thought to reduce overactive brain activity in depression, but the investi…
Many people with depression do not get better with standard treatments like medication. One promising alternative is transcranial magnetic stimulation (TMS), a non-invasive procedure that uses magnetic pulses to stimulate specific brain regions. A particular pattern of TMS called continuous theta-burst stimulation (cTBS) is thought to reduce overactive brain activity in depression, but the investigators do not yet fully understand how it works at the level of brain cells and connections.
This study aims to determine the biological mechanism by which cTBS changes brain activity in people with depression. Specifically, the investigators are testing two competing ideas: (1) that cTBS works by weakening the connections between brain cells through a process called long-term depression (LTD), which is driven by a chemical messenger system called glutamate; or (2) that cTBS works by increasing the brain's natural "braking" system, driven by a different chemical messenger called GABA.
To test these ideas, participants with depression will receive cTBS along with one of four FDA-approved medications, or placebo, that either boost or block these chemical messenger systems. The investigators will measure changes in brain activity using electroencephalography (EEG) recorded simultaneously with TMS. Specific patterns in the EEG signal, called TMS-evoked potentials (TEPs), act as a window into how different brain cell types are responding to stimulation.
Each participant will complete four study visits, each testing a different drug-TMS combination in random order. One group of participants will test drugs targeting the glutamate system (d-cycloserine and memantine). A second group will test drugs targeting the GABA system (lorazepam and baclofen). All drugs are given as a single oral dose and are commonly used in clinical practice.
Understanding exactly how cTBS works at a biological level could open the door to more effective, personalized TMS treatments.
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Eligibility Criteria
Inclusion Criteria:
* Can safely receive TMS and study drugs
* Stable medication regimen for one month prior to study participation, and for the duration of the study
* Not currently receiving TMS, ECT, or ketamine
* No active safety concerns related to suicidality
* Moderate to severe Major Depres…
Inclusion Criteria:
* Can safely receive TMS and study drugs
* Stable medication regimen for one month prior to study participation, and for the duration of the study
* Not currently receiving TMS, ECT, or ketamine
* No active safety concerns related to suicidality
* Moderate to severe Major Depressive Disorder as indicated by the Patient Health Questionnaire or Quick Inventory of Depressive Symptomatology
Exclusion Criteria:
* History of seizures or epilepsy
* History of intracranial pathology or lesions from any etiology
* History of traumatic brain injury including prolonged loss of consciousness more than 15 min
* Signs of increased intracranial pressure
* Any major neurological conditions (ex: recent stroke, tumor, neurodegenerative disorders, etc.)
* Major medical conditions that may cause a medical emergency in case of a provoked seizure (cardiac malformation, cardiac dysrhythmia, asthma, etc.)
* Severe migraines that may result in treatment intolerance.
* Inability to tolerate MRI.
* Pregnancy
* Known allergic reaction to d-cycloserine, baclofen, memantine, or lorazepam
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