Clinical Study

A Randomized, Double Blind, Placebo Controlled, Parallel-Group Study to Evaluate the Safety and Efficacy of Curene® versus Placebo in Reducing Symptoms of Knee OA

Table 4

Mean change from baseline in total WOMAC.

VisitsCurene® 500mgPlacebo
N=25N=25
Mean (SD)Change from baselineMean (SD)Change from baseline

Baseline (Day 0)37.88±4.1437.36±4.08
Visit 2 (Day 7)34.88±5.273±1.5536.4±3.880.96±1.77
Visit 3 (Day 15)31.44±4.856.44±1.5034.36±3.793±2.22
Visit 4 (Day 30)25.84±5.5412.04±2.8932.76±3.884.6±2.81
Visit 5 (Day 60)18.44±4.7519.44±3.7430.76±4.846.6±3.66

Statistically significant (P <0.05) within group; ∧ statistically significant (P <0.05) between group.
Within group analysis by Pair t-test and between group analysis by repeated measures ANCOVA.