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. 2011 Jun 27;366(1572):1879–1888. doi: 10.1098/rstb.2010.0394

Table 1.

Gender comparison of nocebo rates in pharmacological trials of depression and anxiety disorders. n, total sample size in the placebo group; ktotal, total number of placebo groups reporting the symptom; 95% CI, confidence interval of odds ratio; modified from Nestoriuc & Rief [56].

symptom diagnosis: depression
diagnosis: anxiety disorder
n (ktotal) odds ratioa 95% CI n (ktotal) odds ratioa 95% CI
loss of appetite 505 (9) 13.2 (6.6; 47.9) 264 (5) 0.3 (0.02; 1.3)
sexual problems 803 (5) 4.0 (1.6; 9.8) 451 (8) 0.2 (0.09; 0.6)
sweating 549 (5) 12.5 (6.0; 26.1) 309 (5) 0.2 (0.06; 0.5)
dry mouth 310 (12) 0.6 (0.1; 2.6) 527 (13) 0.7 (0.42; 1.2)
nausea 1291 (18) 2.3 (1.18; 4.7) 791 (14) 0.5 (0.3; 0.8)
dizziness 773 (11) 10.5 (6.2; 18.0) 269 (7) 0.3 (0.2; 0.6)
drowsiness 1062 (10) 6.7 (4.1; 11.1) 551 (8) 0.5 (0.3; 0.9)
insomnia 1009 (13) 1.9 (0.6; 5.6) 701 (11) 0.4 (0.2; 0.5)
nervousness 197 (6) 3.4 (1.1; 10.1) 299 (7) 0.3 (0.2; 0.7)
diarrhoea 944 (7) 4.1 (2.6; 6.5) 406 (6) 0.8 (0.5; 1.5)
headache 830 (12) 3.1 (1.3; 7.6) 586 (11) 0.6 (0.4; 0.9)

aNocebo rates from studies with high rates of female patients (greater than 66.6%) in relation to studies with high rates of male patients (greater than 66.6%); odds ratios higher than one denote higher nocebo rates in men, odds ratios smaller than one denote higher nocebo rates in women; significant effects are denoted in bold.