Ketamine and Esketamine for Major Depressive Disorder

Long-Term Maintenance With Ketamine and Esketamine for Reduction of Suicide in High-Risk Patients With Depression

Recruiting Phase 4 Interventional Study
Major Depressive Disorder
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Prior Safety Data This treatment has already been tested in at least one earlier human trial.
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Review the details below, then apply to join this clinical trial.

At a Glance
Age
18 – 70
Sex
Any
Trial phase
Phase 4
Study type
Interventional
Purpose
Treatment
Participants needed
100 (estimated)
Sponsor
Massachusetts General Hospital · Other
Who this trial is looking for

This trial is looking for patients with major depression who have thoughts of suicide. Participants will receive treatments of ketamine and esketamine over 24 weeks while answering surveys and attending assessments.

Are You a Good Fit for This Trial?
Rules you out Severe liver diseaseSevere kidney diseaseUncontrolled hypertensionUncontrolled hyperthyroidismBipolar disorderPsychotic symptoms

You may be able to join if

  • I am an inpatient at a psychiatric unit.
  • I am 18 to 70 years old.
  • I have been diagnosed with major depressive disorder.
  • I have been experiencing a major depressive episode for at least 8 weeks.
  • I have thoughts of suicide.
  • I am in good general health.
  • I have access to a mobile phone or computer with internet.
  • I can provide written consent for this trial.

You may not be able to join if

  • I have received IV ketamine treatment before.
  • I am pregnant or breastfeeding.
  • I have an unstable medical condition.
  • I currently have a moderate to severe substance use disorder.
  • I have bipolar disorder or psychotic symptoms.
  • I am receiving ECT treatment.
  • I have significant cognitive impairment.
  • I have uncontrolled hypertension.

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.

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About This Trial
The study will consist of a 24-week-long trial examining outcomes in patients with Major Depressive Disorder and suicidal ideation who will receive intravenous (IV) ketamine and intranasal (IN) esketamine, compared to a large sample of matched historical controls. Patients will be recruited from an inpatient psychiatric unit. Eligible patients who provided informed consent will be enrolled in the …
Trial Locations
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Eligibility Criteria
Inclusion Criteria: 1. Inpatient at a psychiatric unit (or MGH medical unit, awaiting transfer to psychiatry). 2. Male and female, 18-70 years of age, inclusive, at screening. 3. Diagnosis of MDD, single or recurrent, and currently experiencing a major depressive episode (MDE) at least eight weeks …
Contacts

Cristina Cusin, MD

617-724-5510

mghketamindstudy@partners.org

CONTACT

Catherine Schuessler, BS

617-643-7690

mghketamindstudy@partners.org

CONTACT