RecruitingPhase 2NCT05786066

The Impact of AMPA Receptor Blockade on Ketamine's Anti-Suicidal Effects


Sponsor

Yale University

Enrollment

30 participants

Start Date

Apr 3, 2023

Study Type

INTERVENTIONAL

Conditions

Summary

The purpose of this study is to test the hypothesis that the anti-depressant and anti-suicidal effects of the N-methyl-D-aspartate receptor (NMDAR) antagonist Ketamine is critically dependent on stimulation of Alpha-Amino-3-Hydroxy-5-Methyl-4-Isoxazole Propionic Acid receptors (AMPAR).


Eligibility

Min Age: 21 YearsMax Age: 65 Years

Plain Language Summary

Simplified for easier understanding

This study is investigating whether blocking a specific brain receptor (the AMPA receptor) affects how well ketamine reduces suicidal thoughts in people with treatment-resistant depression. Ketamine is a medication that can rapidly reduce suicidal thoughts, but researchers don't fully understand why. This study aims to find out. **You may be eligible if...** - You are 18 or older with a current diagnosis of major depression, PTSD, or bipolar disorder - You have significant depressive symptoms and current suicidal thoughts - Your depression has not responded to at least one antidepressant medication - You are currently receiving mental health treatment - Your current medications have been stable for at least 4 weeks **You may NOT be eligible if...** - You have a history of psychosis, schizophrenia, or certain other serious psychiatric conditions - You have moderate-to-severe substance use disorder - You have serious, unstable heart or liver problems - You are pregnant or breastfeeding - You are not currently engaged with a mental health provider Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGPerampanel 6 MG

Perampanel will be administered 2.5 hours before Ketamine infusion

DRUGKetamine

Ketamine infusion (0.5 mg/kg infusion over 40 minutes) will be administered 2.5 hours post perampanel or placebo administration.

DRUGPlacebo

Placebo will be administered 2.5 hours before Ketamine infusion


Locations(1)

VA Connecticut Healthcare System

West Haven, Connecticut, United States

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NCT05786066


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