This interventional trial (n=20) aims to conduct repeated neurocognitive measurements in depressed patients, treated with ketamine, specifically those with unipolar depression.
Led by Jay Fournier from Ohio State University, the study plans to commence in May 2024. The primary goal is to track the functioning of potential neurobiological targets for depression over time and examine their relationship with real-world functioning. Additionally, a subset of participants will receive a single dose of intravenous ketamine to determine its effect on these targets.
Participants must be between 18 and 60 years old and have a Hamilton Depression Rating Scale (Ham-D) score of at least 14. Exclusion criteria include conditions such as bipolar disorder, substance use disorder, and acute suicidality.
The primary outcome measure will be fMRI resting-state connectivity, assessed 24 hours post-intervention. Secondary outcome measures include depression ratings using the Montgomery-Asberg Depression Rating Scale and the Hamilton Depression Rating Scale at various time points post-intervention. The study is expected to conclude in December 2025.
Trial Details
In this project, we will A) track the functioning of a collection of potential neurobiological targets for depression over time, B) examine how fluctuations in the functioning of those targets relates to real-world functioning, and C) in a subset of the sample, determine how the functioning in those targets is altered by a single dose of ketamine.Trial Number NCT05991232
Sponsors & Collaborators
Ohio State UniversityThe Center for Psychedelic Drug Research & Education (CPDRE) at the College of Social Work at Ohio State University aims to explore and advance the research about psychedelic drugs and their effects, and to disseminate the knowledge about psychedelics.