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Table 3 Efficacy analysis

From: The antipyretic efficacy and safety of propacetamol compared with dexibuprofen in febrile children: a multicenter, randomized, double-blind, comparative, phase 3 clinical trial

Efficacy variable

Study group (n = 125)

Control group (n = 138)

p-value

AUC of BT change at 6 h after administration-and-time relationship

5.98 ± 3.87

5.78 ± 4.01

0.683

BT reduction at 4 h after administration (°C)

0.97 ± 0.90

1.16 ± 0.92

0.09

Maximum value of BT reduction during the 6 h after administration (°C)

1.63 ± 0.66

1.64 ± 0.70

0.855

Number of patients whose BT normalized (< 37.0 °C) at 6 h after administration, n (%)

26 (20.8)

23 (16.7)

0.390

Time point when BT first reached < 37.0 °C, hour

1.73 ± 1.29

2.13 ± 1.06

0.064

  1. Results are presented as mean ± standard deviation or as a percentage (%)
  2. BT Body Temperature
  3. AUC Area Under the Curve