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A randomized, double-blind, active-controlled, double-dummy, parallel-group study to determine the safety and efficacy of oxycodone/naloxone prolonged-release tablets in patients with moderate/severe, chronic cancer pain

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Figure

Figure 1. (a) Patient disposition; (b) study populations. The double-blind safety population included all patients who received any doseof study medication; the full-analysis population I excluded one patient from the double-blind safety population who did
Table 1. Patient demographics and clinical characteristics (double-blind safety population)
Figure 2. Effect of OXN PR and OxyPR treatment on (a) mean (represent standard error; OXN(b) mean (model
Table 2. Patient assessment of constipation using PAC-SYM(Full-Analysis II population)
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