Ketamine's brain impact revealed in small stanford study
NCT ID NCT03475277
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This completed Stanford study looked at how ketamine changes activity in brain areas linked to reward and risk. Thirteen healthy adults who had used ketamine before underwent brain scans while performing tasks. The goal was to understand ketamine's effects on brain circuits, not to treat any disease.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Ketamine
- What this could lead to
- If successful, this could help explain how ketamine alters brain reward pathways, potentially guiding future treatments for addiction or mood disorders.
- What could go wrong
- This is a very small, early biomarker study with only 13 healthy participants, so results may not apply to broader populations or lead directly to treatments.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
-
13 people
The number who actually took part.
- Started
-
Aug 2019
- Finished
-
Jul 2024
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Healthy volunteers with prior exposure to ketamine
- Ages
-
18 to 55 years
- Sex
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Anyone
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Ages 18-55 years * At least 2 prior uses of ketamine when aged 18+ * BMI within healthy range (18-30) * Ability to speak, read, or understand English Exclusion Criteria: * Current active suicide ideation or history of suicide attempts * Current mood, anxiety, eating, psychotic, or substance use disorder * Lifetime psychotic or bipolar disorder * Schizophrenia in a first degree relative * Current use of psychotropic medication * Prior adverse ketamine response * Allergy or hypersensitivity to ketamine * Use of ketamine in past 7 days * Cannabis use in the past 7 days, illicit recreational drug use in the 48 hours prior to sessions, and/or alcohol use in the 24 hours prior to sessions * Concurrent use of any medications that might increase the risk of participation (e.g., drug interactions) * History of epilepsy, convulsions, seizures, LOC \>10 min * Renal/hepatic impairment * Hypertension (Stage 1 defined as systolic blood pressure \>140 mmHg or diastolic blood pressure \>90 mmHg on 2 of 3 measurements at least 15 min apart at initial screening; systolic blood pressure \>155 mmHg or diastolic blood pressure \>99 mmHg on 2 of 3 measurements at least 15 min apart during infusion visits) * Heart rate \<50 bpm or \>150 bpm at initial screening * Chronic congestive heart failure, tachyarrhythmias, myocardial ischemia assessed via EKG at initial screening * EKG QTcF intervals \>430 ms for men and \>470 ms for women * Direct physical access to or routine handling of addicting drugs in the regular course of work duties * MRI contraindication * Pregnant or nursing females
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As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Stanford Psychiatry
Palo Alto, California, 94304, United States
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