Primary Outcomes | Parecoxib group | Placebo group | RR (95% CI) | P value |
---|
CPSP at 3 mo, N (%) | 18 (35.3) | 24 (44.4) | 0.794 (0.493 ~ 1.279) | 0.34 |
Worst-case scenarioa | 23 (45.1) | 24 (44.4) | 1.015 (0.663 ~ 1.552) | 0.95 |
Per-protocol analysisb | 18 (39.1) | 24 (49.0) | 0.799 (0.504 ~ 1.265) | 0.33 |
- CPSP chronic post-surgical pain; CI confidence interval; RR relative risk
- a All patients lost to follow-up in the parecoxib group developed CPSP, while all patients lost to follow-up in the placebo group did not develop the condition
- b Only patients who received allocated intervention and completed follow-up were included in his study