RecruitingPhase 1NCT05915013

Alpha-Amino-3-Hydroxy-5-Methyl-4- Isoxazole Propionic Acid Receptor Components of the Anti-Depressant Ketamine Response


Sponsor

Yale University

Enrollment

50 participants

Start Date

Sep 7, 2023

Study Type

INTERVENTIONAL

Conditions

Summary

The proposed study will assess the combined effect of perampanel and ketamine on the anti-depressant response in individuals with treatment resistant depression. The purpose of this study is to test the hypothesis that stimulation of Alpha-Amino-3-Hydroxy-5-Methyl-4- Isoxazole Propionic Acid receptors (AMPAR) is critical to the anti-depressant response of ketamine.


Eligibility

Min Age: 18 YearsMax Age: 60 Years

Plain Language Summary

Simplified for easier understanding

This study is investigating how ketamine relieves severe, treatment-resistant depression — specifically looking at whether AMPA receptors (a type of brain signaling pathway) play a key role in its rapid antidepressant effect. **You may be eligible if...** - You are right-handed (required for brain scan accuracy) - You currently have depression with a Hamilton score above 17 - You have treatment-resistant depression (failed at least one antidepressant) - You are 18 or older **You may NOT be eligible if...** - You have a history of psychosis, bipolar disorder, or substance use disorder - You have significant heart, brain, or neurological conditions - You are pregnant or breastfeeding - You are currently taking medications that interact with ketamine 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

DRUGKetamine

Intravenous ketamine

DRUGPerampanel

Oral perampanel (6 mg)

DRUGPlacebo

Oral placebo


Locations(1)

Yale University

New Haven, Connecticut, United States

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NCT05915013


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