Knee OA Patients on Apos® Show Both Subjective and Objective Improvement

A study comparing knee OA patients who received Apos® against a control group found that Apos® patients did better in both patient-reported (subjective) clinical measures and functional test (objective) measures. Moreover, the Apos® group reported a significant reduction in painkiller consumption.

A randomized controlled trial study in A controlled, double-blind study examined the effect of Apos® on the clinical results of subjects with knee OA. The study examined the changes in patient-reported outcome measures (PROMs) and in functional tests, among subjects who were assigned to Apos®, compared with a control group.

Apos® was found to be superior regarding reduction in pain and improvement in function and quality of life. Furthermore, compared to the control group, subjects assigned to Apos® reported a reduction of over 50% in the consumption of over-the-counter painkillers.

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