Table 2.
Comparison of the efficacy and safety of treatment in the three groups
Variable | A group (n = 73) | B group (n = 71) | C group (n = 72) | X2 | P |
---|---|---|---|---|---|
Therapeutic efficacy n (%) abc | |||||
Complete normalization individual quantity | 61(83.6%) | 47(66.2%) | 44(61.1%) | ||
Partial improvement individual quantity | 4(5.5%) | 7(9.9%) | 8(11.1%) | 9.612 | 0.008 |
No improvement individual quantity | 8(10.9%) | 17(23.9%) | 20(27.8%) | ||
Safety n (%) with adverse reactions | |||||
Mild | 5(6.85%) | 6(8.45%) | 5(6.94%) | 0.168 | 0.919 |
Moderate | 1(1.4%) | 1(1.4%) | 1(1.4%) | 0.000 | 1.000 |
Severe | 0(0%) | 0(0%) | 0(0%) |
A group received bicyclol tablets, B group received diammonium glycyrrhizinate enteric–coated capsules, and C group received silibinin capsules.
Statistical significance of differences between groups in therapeutic efficacy:
a : A vs B, significant (P = 0.016).
b: A vs C, very significant (P = 0.003).
c: B vs C, not statistically significant (P = 0.531).