Early Phase 1 Depression and Anxiety Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- People who are medically able to safely receive TMS (a type of brain stimulation) and the study medications.
- People whose medication routine has been stable for at least one month before the study and who are able to keep it stable throughout the study.
- People who are not currently receiving TMS, ECT (electroconvulsive therapy), or ketamine treatment.
- People who do not have active safety concerns related to suicidal thoughts or behaviours.
- People with moderate to severe Major Depressive Disorder, as measured by a standard depression questionnaire.
Who may not be able to join:
- People with a history of seizures or epilepsy.
- People with a history of any condition, injury, or abnormality affecting the inside of the skull or brain.
- People with a history of traumatic brain injury that involved loss of consciousness lasting more than 15 minutes.
- People who show signs of increased pressure inside the skull.
- People with a significant neurological condition, such as a recent stroke, brain tumour, or a degenerative brain disease (confirm with trial site for full list).
- People with serious medical conditions that could become dangerous if a seizure were to occur, such as certain heart or breathing conditions (confirm with trial site for full list).
- People with severe migraines that may make it difficult to tolerate the treatment.
- People who are unable to tolerate an MRI scan.
- People who are pregnant.
- People with a known allergic reaction to any of the following study drugs: d-cycloserine, baclofen, memantine, or lorazepam.
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Joshua C Brown, MD, PhD, Mclean Hospital
Phone: 617-855-2153
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Change in P30 TEP Peak Amplitude; Change in N45 TEP Peak Amplitude; Change in N100 TEP Peak Amplitude
Can't join this trial?
Data last synced from ClinicalTrials.gov: 21 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.