Skip to main content

Table 5 Efficacy results in patients treated with lumiracoxib and rofecoxib (ITT population)

From: A 6-week, multicentre, randomised, double-blind, double-dummy, active-controlled, clinical safety study of lumiracoxib and rofecoxib in osteoarthritis patients

 

Week 3

Week 6

Efficacy measures

Lumiracoxib 400 mg od

( n = 154)

Rofecoxib 25 mg od

( n = 155)

Lumiracoxib 400 mg od

( n = 154)

Rofecoxib 25 mg od

( n = 155)

Patient's pain intensity

    

   Improved n (%)

53 (34.4)

50 (32.3)

49 (31.8)

63 (40.6)

   Non-improved n (%)

101 (65.6)

105 (67.7)

105 (68.2)

92 (59.4)

Patient's global assessment of disease activity

    

   Improved n (%)

49 (31.8)

53 (34.2)

57 (37.0)

65 (41.9)

   Non-improved n (%)

105 (68.2)

102 (65.8)

97 (63.0)

90 (58.1)

Physician's global assessment of disease activity

    

   Improved n (%)

44 (28.6)

46 (29.7)

51 (33.1)

56 (36.1)

   Non-improved n (%)

110 (71.4)

109 (70.3)

103 (66.9)

99 (63.9)