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. 2020 Aug 7;35(6):305–312. doi: 10.1097/YIC.0000000000000326

Table 1.

Demographic and baseline clinical characteristics

Vortioxetine (n = 39) Placebo (n = 41)
Demographic and clinical characteristics
Women, n (%) 28 (71.8) 30 (73.2)
Age (years) 47.3 (11.0) 46.9 (13.7)
Ethnicity, n (%)
 Caucasian 39 (100) 40 (97.6)
 Black or African-American 0 1 (2.4)
BMI (kg/m2) 25.0 (3.7) 24.6 (3.5)
Duration of current episode (days) 150.6 (50.2) 165.5 (77.1)
 Median (days) 140 131
Number of previous episodes 3.4 (2.0) 2.8 (1.7)
 Range 1-10 1-8
Treatment at study entry
 SSRI, n (%) 26 (66.7) 29 (70.7)
 SNRI, n (%) 13 (23.3) 12 (29.3)
Baseline clinical assessments
MADRS total score 35.6 (3.4) 34.7 (2.7)
MADRS-6 subscale score 23.4 (2.3) 22.9 (2.2)
CGI-S score 5.1 (0.6) 5.1 (0.5)
HADS-D score 16.5 (3.2) 15.7 (3.2)
HADS-A score 12.1 (3.0) 11.8 (3.6)
PGIC score 1.4 (0.6) 1.5 (0.6)

Mean (SD) reported unless otherwise specified. Demographic and clinical characteristics based on all treated patients; clinical assessments based on the full-analysis set.

CGI-I, Clinical Global Impressions – Improvement; CGI-S, Hospital Anxiety and Depression Scale – Depression; HADS-A, Hospital Anxiety and Depression Scale – Anxiety; MADRS, Montgomery–Åsberg Depression Scale; PGI-C, patient global impression of change; SNRI, serotonin-norepinephrine reuptake inhibitors; SSRI, selective serotonin reuptake inhibitors.