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. 2024 Jun 17;165(11):2578–2585. doi: 10.1097/j.pain.0000000000003291

Table 1.

Demographics of placebo response study population.

Variable Lidocaine (n = 26) Control (n = 25) Total (n = 51)
Age, y (mean, SD) 51 (15) 54 (17) 53.4 (15)
Sex, F (N, %) 17 (65%) 16 (64%) 33 (64.7%)
Diagnosis, (N, %)
 EIA 1 (4%) 1 (4%) 2 (3.9%)
 Seropositive RA 10 (38%) 8 (32%) 18 (35.2%)
 Seronegative RA 7 (27%) 6 (24%) 13 (25.4%)
 PsA 3 (12%) 7 (28%) 10 (19.6%)
 Peripheral SpA 4 (15%) 1 (4%) 5 (9.8%)
 JIA 1 (4%) 1 (4%) 2 (3.9%)
 IBD-related arthritis 0 (0%) 1 (4%) 1 (2.0%)
Preinjection pain NRS score, mean (SD) 7.2 (2.0) 6.4 (2.5) 6.9 (2.3)
Joint
 Knee 14 (54%) 15 (60%) 29 (57%)
 Wrist 7 (27%) 7 (28%) 14 (28%)
 Elbow 1 (4%) 3 (12%) 4 (8%)
 Ankle 3 (12%) 0 (0%) 3 (6%)
 MCP 1 (4%) 0 (0%) 1 (2%)
Fluid off (mLs), mean (SD) 7.2 (13) 8.5 (20) 7.8 (16)
PainDETECT score, mean (SD) 16 (9.4) 13 (8.0) 14.7 (8.7)

Means presented with SD. There was no significant difference between variables presented in lidocaine and control group.