Exploring how ketamine affects memory and emotions in depression
Does Modulation of Glutamate Transmission in the Brain Using a Sub-anaesthetic Dose of Ketamine Affect Autobiographical Memory, Emotional Processing and Decision-making in Treatment-resistant Depression?
NA · University of Oxford · NCT05809609
This study is testing how ketamine affects memory and emotions in people with depression who haven't found relief from other treatments.
Quick facts
| Phase | NA |
|---|---|
| Study type | Interventional |
| Enrollment | 60 (estimated) |
| Ages | 20 Years to 60 Years |
| Sex | All |
| Sponsor | University of Oxford (other) |
| Locations | 1 site (Oxford) |
| Trial ID | NCT05809609 on ClinicalTrials.gov |
What this trial studies
This study investigates the effects of ketamine on memory reconsolidation and emotional processing in individuals with treatment-resistant depression. Participants will undergo medical and psychiatric screenings and receive either ketamine or a placebo. The research aims to understand how ketamine influences the way depressed individuals recall past experiences and process emotions related to rewards and punishments. By elucidating the mechanisms of ketamine's action, the study seeks to contribute to the development of rapid-acting antidepressants targeting the glutamatergic system.
Who should consider this trial
Good fit: Ideal candidates are adults diagnosed with Major Depressive Disorder who have not responded adequately to standard antidepressant treatments.
Not a fit: Patients who are not currently experiencing a major depressive episode or those who have not tried at least one antidepressant may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved treatment options for patients suffering from treatment-resistant depression.
How similar studies have performed: Previous studies have shown promising results with ketamine in treating depression, indicating potential success for this approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Willing and able to give informed consent for participation in the study * Sufficiently fluent English to understand and complete the tasks * Registered with a GP and consents to GP being informed of participation in the study Participants need to meet a number of concurrent clinical criteria: * Current criteria for Major Depressive Disorder, in a current major depressive episode as determined by the SCID-5. * Inadequate response to at least one and no more than three antidepressant treatments. * Currently taking a licensed antidepressant at a therapeutic dose for at least four weeks. * Pre-menopausal women and male participants engaging in sex with a risk of pregnancy must agree to use a highly effective method of contraception from Screening Visit until 30 days after receiving the study medication treatment. Acceptable methods of contraception include: * Condoms * Combined (estrogen- and progestogen-containing) hormonal contraception associated with inhibition of ovulation: oral, intravaginal or transdermal * Progestogen-only hormonal contraception associated with inhibition of ovulation oral, injectable or implantable * Intrauterine device (IUD) * Intrauterine hormone-releasing system (IUS) * Bilateral tubal occlusion * Vasectomy (or vasectomised partner) * Sexual abstinence. \[Periodic abstinence (calendar, symptothermal, post-ovulation methods), withdrawal (coitus interruptus), and spermicides only are not acceptable methods of contraception.\] * Male participants must not donate sperm until 30 days after receiving the study medication. * Participants taking non-prescription/prescription medication may still be entered into the study, if, in the opinion of the Investigator, the medication received will not interfere with the study procedures or compromise safety * Willingness to refrain from driving, cycling, or operating heavy machinery, until the following morning or a restful sleep has occurred, whichever is later. * Willingness to refrain from drinking alcohol for 3 days before the infusion visit and one day before any of the other visits throughout the study. Exclusion Criteria: * The participant may not enter the study if ANY of the following apply: * History of /or current DSM-5 bipolar disorder, schizophrenia or emotionally unstable personality disorder \[co-morbid anxiety disorders (including agoraphobia, generalized anxiety disorder, social anxiety disorder and panic disorder) and Posttraumatic Stress Disorder (PTSD) are allowed\] * Participants who fulfil current criteria for other comorbid disorders may still be entered into the study, if, in the opinion of the Investigator, the psychiatric diagnosis will not compromise safety or affect data quality * Diagnosis of a major cognitive disorder or evidence of cognitive impairment * Clinically significant risk of suicide * Participants undergoing or who have undergone electroconvulsive therapy for the treatment of the current episode of depression * Substance or alcohol use disorder over the past 6 months * Regular alcohol consumption of more than 21 units a week or excessive alcohol consumption up to three days before any of the in-person study visits or inability to abstain from alcohol for more than 3 days * Moderate cigarette use (\> 10 cigarettes per day) * History of, or current general medical conditions that in the opinion of the Investigator may interfere with the safety of the participant or the scientific integrity of the study * Current pregnancy (as determined by urine pregnancy test), breastfeeding, planning a pregnancy, or unwillingness to practice birth control during the course of the study * Clinically significant abnormalities of laboratory tests, physical examination, or ECG. A participant with a clinical abnormality or parameters outside the reference range for the population being studied may be included only if the Investigator considers that the finding is unlikely to introduce additional risk factors and will not interfere with the study procedures * Current or past history of heart rhythm disorders * Clinically significant untreated hypertension * Any contraindication to MRI including claustrophobia, any trauma or surgery which may have left magnetic material in the body, magnetic implants or pacemakers, and inability to lie still for 1 hour or more * Previous participation in a study using the same, or similar, emotional processing tasks in the last three months * Previous lifetime use of ketamine or phencyclidine * Participant with planned medical treatment within the study period that might interfere with the study procedures * Participant who is unlikely to comply with the clinical study protocol or is unsuitable for any other reason, in the opinion of the Investigator.
Where this trial is running
Oxford
- Department of Psychiatry, University of Oxford — Oxford, United Kingdom (RECRUITING)
Study contacts
- Principal investigator: Catherine Harmer, DPhil — University of Oxford
- Study coordinator: Sara Costi, MD
- Email: sara.costi@psych.ox.ac.uk
- Phone: 01865 618303
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions: Treatment Resistant Depression, Depression, Major Depressive Disorder, Ketamine, Memory, Mental Health, Learning