Abstract
19 men and 61 women with degenerative arthritis of the knee joint were randomly allocated to receive tenoxicam 20mg (n = 40) or piroxicam 20mg (n = 40) orally before breakfast once daily, for 6 weeks. The study was of a double-blind parallel design and patients underwent a washout period of up to 14 days before beginning the study medications. The 2 groups were of comparable sex ratio, age, weight, disease duration and treatment history, with most patients having a 1to lO-year history of disease and 48 patients having previ-
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