Severe Depression
Conditions
Keywords
fMRI, psilocybin, ketamine, biomarker, rapid-acting antidepressants
Brief summary
The main aim of the study is to investigate the possible long-term therapeutic effects of psilocybin on the symptoms of severe depression, as well as the brain mechanisms underlying these changes. Depression severity is assessed before and after (i.e., 1 week, 3 months and 6 months after) a single dose of psilocybin and compared to respective scores of a group receiving an active placebo, ketamine. Brain activity (using functional magnetic resonance imaging) is measured before and one week after drug administration in order to determine whether changes in brain networks related to emotional and self-referential processing correlate with any observed changes in depression scores. Further, blood samples will be obtained from the participants and analyzed in order to reveal gene expression and molecular level correlates underlying rapid antidepressant effects, and to identify biomarkers that predict treatment outcome.
Interventions
DRUGPsilocybin
Psilocybin ingested orally
Ketamine administered intranasally
Sponsors
Dr. Tomi Rantamäki, Laboratory of Neurotherapeutics, Department of Biosciences, University of Helsinki
Dr. Robin Carthart-Harris and Prof. David Nutt, Imperial College London, UK
University of Helsinki
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)
Masking description
Since the psilocybin is ingested orally in capsule form, whereas ketamine is administered intranasally, the participants will either receive a placebo capsule containing microcrystalline cellulose (if they belong to the group receiving ketamine), or intranasally administered saline solution (with added bitter flavoring which will mimic the taste of ketamine that is often detectable even when administered intranasally).
Intervention model description
In a randomized, double-blind placebo-controlled design, 20 of the participants will receive ketamine, and 20 will receive psilocybin. 20 of the participants will be included in the study as a no-treatment group, so that natural time-dependent changes in depressive symptoms can be controlled for and thus the antidepressive effects of ketamine and psilocybin treatment can be verified. The no-treatment group will only attend the initial clinical interviews, and their depressive symptoms will be assessed remotely.
Eligibility
Sex/Gender
ALL
Age
18 Years to 64 Years
Healthy volunteers
No
Inclusion criteria
1. Major depression of a moderate to severe degree (17+ on the 21-item HAM-D). 2. No health-related contraindications.
Exclusion criteria
1. Current or previously diagnosed psychotic disorder. 2. Immediate family member with a diagnosed psychotic disorder. 3. Medically significant condition rendering unsuitability for the study (e.g., diabetes, epilepsy, severe cardiovascular disease, hepatic or renal failure etc.). 4. History of suicide attempts. 5. History of mania. 6. Current 5-HT2A antagonist antidepressant medication. 7. Blood or needle phobia. 8. Positive pregnancy test. 9. Current drug or alcohol dependence. 10. Lack of appropriate use of contraception. 11. Breast-feeding.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| The 16-Item Quick Inventory of Depressive Symptomatology (QIDS) | 6 months | The primary outcome measures in this study will be the mean change in QIDS scores from pre-administration baseline at day 1 to Follow-up 2 at day 103 (3 months after the administration session). Additionally, an electronic version of the QIDS will be performed 6 months after the administration session. The criteria for determining response will be a reduction of 25% in the (QIDS; Rush et al., 2003) scores from baseline (screening), and remission will be scores of ≤5 on the QIDS. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| The Montgomery and Asberg Depression Rating Scale | 3 months | The Montgomery and Asberg Depression Rating Scale will be carried out at screening ( day 1), Follow-up 1 (day 18) and Follow-up 2 (day 103, 3 months after the administration session). |
| Hamilton Depression Rating Scale | 3 months | The Hamilton Depression Rating Scale will be carried out at screening ( day 1), Follow-up 1 (day 18) and Follow-up 2 (day 103, 3 months after the administration session). |
Contacts
Primary ContactMona E Moisala, PhD
Outcome results
None listed