Clinical Study

Clinical Evaluation of a Novel Technology for Oral Patient-Controlled Analgesia, the PCoA® Acute Device, for Hospitalized Patients with Postoperative Pain, in Pilot Feasibility Study

Table 4

Analysis of total pills administered by group. Analysis was done by nonparametric Wilcoxon-Mann–Whitney. Analysis of variance (ANOVA model) was applied for analyzing the difference in the study outcomes between study centers within study groups (MC: Medical Center).

ParameterAll centersMC-AMC-BMC-C
GroupControl TestControl TestControl TestControl Test

Number of total pills75135215517493731
Number of patients4327209129119
Parameter (number of pills/ patient)
Mean1.675.000.956.111.425.443.273.44
Std2.282.421.962.711.781.942.651.88
Min0.001.000.003.000.002.000.001.00
Median1.006.000.006.000.506.003.004.00
Max8.0012.008.0012.005.007.007.007.00
Lower 95% confidence limit0.974.040.034.030.283.951.492.00
Upper 95% confidence limit2.375.961.878.202.556.945.054.89
value (Wilcoxon test) <0.0001
value for difference between the centers by group (ANOVA)Control:  
Study: