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.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
OTHER
Masking
TRIPLE
Enrollment
40
Nitrous oxide will be administered at an inspiratory concentration of 50% with concurrent intravenous saline (100ml) for one hour.
Oxygen will be administered at 50% with intravenous midazolam (0.02mg/kg in 100ml) for one hour
St. Michael's Hospital
Toronto, Ontario, Canada
Recruitment rate
Recruitment rate
Time frame: 2 Years
Withdrawal rate
Time frame: 2 Years
Adherence rate
Feasibility
Time frame: 2 Years
Frequency of adverse events
Safety and tolerability
Time frame: 2 Years
Montgomery-Åsberg Depression Rating Scale (MADRAS) Score 0-60 (Higher scores represent higher depression). Measure changes in symptoms of depression
Frequencies on numbers of 1.- Remissions (defined as MADRS score \< 10), 2.- Responses (defined as ≥ 50% reduction in MADRS score from baseline) 3.- No Responses
Time frame: 6 weeks
Toronto Side Effects Scale (TSES) - 32 items (each item has a score 1-25; higher score means higher intensity). Measure adverse side effects from antidepressant treatment
Frequencies of safety and tolerability
Time frame: 6 weeks
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