Overview

Sustained Mood Improvement With Laughing Gas Exposure: A Randomized Controlled Pilot Trial

Status:
Not yet recruiting
Trial end date:
2023-10-01
Target enrollment:
0
Participant gender:
All
Summary
The purpose of the study is to investigate a short-term treatment option for major depressive disorders by administering nitrous oxide gas. At this time, the main purpose is to complete a feasibility study with 40 participants suffering from treatment-resistant depression. Participants will be randomized to (1) Study group: Nitrous oxide (inhaled) + solution of saline (injected) and the (2) Control group: Oxygen (inhaled) + Midazolam (injected) as an Active Placebo.
Phase:
Phase 4
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Karim Ladha
Collaborator:
Unity Health Toronto
Treatments:
Midazolam
Nitrous Oxide
Criteria
Inclusion Criteria:

1. 18 to 65 years of age

2. Meeting Diagnostic and Statistical Manual for Mental Disorders (DSM-5) criteria for
Major Depressive Disorder (MDD)

3. Current major depressive episode as confirmed by the Mini International
Neuropsychiatric Interview (MINI) for DSM-5

4. Experiencing moderate to severe depressive episode, as defined by the Hamilton
Depression Rating Scale (HAMD)>17

5. Failure of two trials of antidepressant therapy of adequate dose and duration, during
the current depressive episode

6. For women of childbearing potential, use of highly effective or double-barrier methods
of contraception. Abstinence is acceptable if it is the preferred and usual lifestyle
of the female participant

7. Capacity to provide informed consent.

Exclusion criteria

1. Acute suicidality defined as score ≥3 on HAMD item 3

2. Major Depressive Episode in people with Bipolar Disorder

3. Current substance abuse or dependence and/or history of alcohol abuse or dependence
within the past year

4. Dementia

5. Current or lifetime history of schizophrenia or schizoaffective disorder

6. Current history of dissociative disorders

7. Known history of hypersensitivity or allergy to Nitrous Oxide, Midazolam or any
ingredients in the study formulations

8. Contraindication to receiving nitrous oxide

9. Chronic cobalamin or folate deficiency

10. Contraindication to receiving the placebo midazolam

11. Use of centrally acting medicinal products, such as opioid agonists, morphine
derivatives, benzodiazepines and/or other central nervous system depressants such as
barbiturates and alcohol

12. Pregnancy or breastfeeding in female participants

13. Electroconvulsive therapy within the current depressive episode

14. Receiving ketamine treatment within the current depressive episode

15. Unwilling to maintain current antidepressant regimen.