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Study identifier: NCT06412315 Synced from ClinicalTrials.gov · July 29, 2026
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7T Amygdala and Citalopram Study

Condition: Emotional Processing · Cognition · Mood Disorders  ·  Sponsor: University of Oxford

PhaseNA
Planned participants50
Who can joinAll sexes, 18 Years to 40 Years
Healthy volunteersYes

About this study

The goal of this study is to investigate how a common antidepressant citalopram (which increases the levels of the chemical messenger serotonin), affects how a key area of the brain involved in depression (the amygdala) responds to emotional information. Healthy participants will undergo medical and psychiatric health screening, after which they will be assigned to receive either a single dose of citalopram (20mg) or placebo, and undergo brain scanning (7T fMRI) whilst viewing emotional faces. Since the scan uses high field strength, the investigators will be able to see effects of citalopram on different subfields within the amygdala which will help to understand how citalopram might be working.

This description comes directly from the study's public registry record.

Talk to the study team

Marieke AG Martens, DPhil  ·  +441865 618338  ·  marieke.martens@psych.ox.ac.uk

Catherine J Harmer, DPhil  ·  +441865 618326  ·  catherine.harmer@psych.ox.ac.uk

Always discuss trial participation with your own doctor first.

Locations (1)

University of Oxford, Department of PsychiatryOxford, Oxfordshire, United KingdomRecruiting

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Source record: clinicaltrials.gov/study/NCT06412315