Skip to main content
. 2012 Nov 29;2012:967968. doi: 10.1155/2012/967968

Table 2.

Changes in VAS scores and pain intensity. (PPS, N = 128).

Variable Group 4 w 8 w 12 w Follow-up period
CXDT-HFG group (n = 86) 4.96 ± 2.01 4.02 ± 2.33 2.39 ± 2.41 1.66 ± 2.15
VAS scores§ Placebo group (n = 42) 4.90 ± 2.09 4.12 ± 2.41 3.21 ± 2.45 2.92 ± 2.51
P* values 0.893 0.679 0.060 0.005

CXDT-HFG group (n = 86)
 No pain, n (%) 7 (8.14%) 15 (17.44%) 37 (43.02%) 49 (56.98%)
 Mild, n (%) 15 (17.44%) 24 (27.91%) 27 (31.40%) 23 (26.74%)
 Moderate, n (%) 57 (66.28%) 43 (50.00%) 21 (24.42%) 13 (15.12%)
 Severe, n (%) 7 (8.14%) 4 (4.65%) 1 (1.16%) 1 (1.16%)
Pain intensity# Placebo group (n = 42)
 No pain, n (%) 4 (9.52%) 8 (19.05%) 12 (28.57%) 16 (38.10%)
 Mild, n (%) 9 (21.43%) 13 (30.95%) 11 (26.19%) 10 (23.81%)
 Moderate, n (%) 25 (59.52%) 19 (45.24%) 19 (45.24%) 16 (38.10%)
 Severe, n (%) 4 (9.52%) 2 (4.76%) 0 (0.00%) 0 (0.00%)
P* values 0.684 0.673 0.037 0.013

W: weeks. Significant difference, P < 0.05. Data presented as mean ± SD, number (percentage).

 *P for comparison with control group.

# P values based on Chi-square test.

§ P values based on repeated measures.

P < 0.05. Statistical differences for comparison between groups.