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RecruitingNCT05915013

Perampanel or placebo alongside ketamine for treatment-resistant depression

About this titleRead the official source — NCT05915013
Medication studyAges 18–60United StatesPTSD
The study in practice

Understand this study

Who could participate?

Listed age limits: 18 years to 60 years.

Listed locations
New HavenSee all locations and recruitment
Study phase
Phase 1Usually an early study focused on safety, tolerability, dosage, and side effects.

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What to know before participating

A point to clarify

This summary does not cover all risks or eligibility requirements. What risks or changes to my care would apply to me?

Study clarity

Things to check before joining

Study start dateStarted: September 7, 2023
Recruitment status
Recruiting
Enrollment listed in the registry
50
Sponsor
Yale University
Sponsor type
University
Study type
Drug
Intervention type
Medication / drug
Study phase
Phase 1Usually an early study focused on safety, tolerability, dosage, and side effects.
Locations
United States
Age range
From 18 Years to 60 Years
Official registry ID
NCT05915013
Official title
Show the full official title

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

Recruitment & locations

Currently recruiting

New Haven

FAQ

Questions about this study

Who is behind this study?

The study sponsor is Yale University, a university.

Does this study involve medication?

Yes. The study involves medication, including ketamine, Perampanel and Placebo.

Who can participate?

Listed age limits: 18 years to 60 years.

Is this study still recruiting?

The registry lists this study as recruiting.

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