Clinical trial aimed at evaluating whether a single infusion of tocilizumab, a medication that blocks the action of an inflammatory molecule called interleukin-6 (IL-6), can reduce symptoms of treatment-resistant major depression compared to placebo in non-hospitalized patients.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Enrollment
32
Single infusion tocilizumab, 8 mg/kg, diluted in 100 mL of normal saline
Placebo, same volume as intervention
Hospital de Clínicas de Porto Alegre
Porto Alegre, Rio Grande do Sul, Brazil
Reduction in depressive symptoms (HDRS)
≥50% reduction in score
Time frame: Baseline and follow-ups (day 7, day 14, day 28 and month 6)
Cognitive performance (Montreal Cognitive Test)
Time frame: Baseline and follow-ups (day 7, day 14, day 28 and month 6)
Quality of life (EUROHISQOL8)
Time frame: Baseline and follow-ups (day 7, day 14, day 28 and month 6)
BDNF levels
Serum Brain-Derived Neurotrophic Factor level
Time frame: Baseline and third follow-up post-intervention (28th day)
ECT indication after invervention
Time frame: Follow-ups (day 7, day 14, day 28 and month 6)
General psychiatric symptoms improvement (BPRS)
Time frame: Baseline and follow-ups (day 7, day 14, day 28 and month 6)
Clinical global improvement (CGI)
Time frame: Baseline and follow-ups (day 7, day 14, day 28 and month 6)
CRP levels
Serum C-Reactive Protein levels
Time frame: Baseline and follow-ups (day 7, day 14, day 28 and month 6)
IL-6 levels
Serum IL-6
Time frame: Baseline (for healthy controls) and baseline and follow-ups for intervention arm(day 7, day 14, day 28 and month 6)
Psychiatric hospitalization rate in 6 months
Time frame: 6 months follow-up
Suicidal ideation (MINI)
Time frame: Elegibility and follow-ups (day 7, day 14, day 28 and month 6)
Quality of life (WHOQOL-BREF)
Time frame: Baseline, follow-ups (day 7, day 14, day 28 and month 6)
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