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Table 2 Demographic and clinical characteristics of the 143 hand OA patients in randomized controlled trial 1 and 2 according to clinically significant improvement

From: Predictors of a placebo response in patients with hand osteoarthritis: post-hoc analysis of two randomized controlled trials

 

Response (−)

(n = 89)

Response (+)

(n = 54)

P-value

Age, years

58.1 ± 7.5

60 ± 8.2

0.164

Female

81 (91.0)

53 (98.1)

0.153

Weight, kg

59.1 ± 8.3

59.9 ± 8.3

0.606

Height, cm

157.3 ± 5.9

155.8 ± 6.2

0.150

BMI, kg/m2

23.9 ± 2.7

24.7 ± 3.1

0.105

OA duration, month

3.2 ± 4

3.5 ± 5.1

0.657

AUSCAN Pain

43.6 ± 21.6

55.7 ± 19.7

0.001

AUSCAN Stiffness

57.5 ± 24.5

68.2 ± 20.5

0.008

AUSCAN Function

41.7 ± 23.2

49.1 ± 26.6

0.083

Patient GA

51.1 ± 16

55.6 ± 19.9

0.158

Physician GA

40.1 ± 11.3

43.7 ± 13.6

0.084

Tender JC

5.8 ± 4.7

6.5 ± 5.7

0.426

Swollen JC

0.8 ± 2.4

0.5 ± 1.5

0.328

Enlarged JC a

5.1 ± 2.7

5.4 ± 2.2

0.622

Deformity JC a

2 ± 1.6

1.9 ± 1.9

0.658

ESR

0.17 ± 0.52

0.09 ± 0.13

0.291

CRP

13.4 ± 10.4

14.5 ± 9.6

0.533

Prior treatment

 Tramadol-AAP a

3 (4.6)

7 (18.9)

0.034

 Tramadol a

1 (1.5)

0 (0)

1.000

 NSAIDs a

22 (33.8)

14 (37.8)

0.685

 Diacerin a

2 (3.1)

1 (2.7)

1.000

 Glucosamine a

9 (13.8)

4 (10.8)

0.765

 Others a

1 (1.5)

2 (5.4)

0.297

  1. Data are presented as the mean (SD) or n (%). P values were generated by using an independent t-test (continuous variables) or the Chi-squared test (categorical variables). a Data were not available in the placebo group of RCT 2. AUSCAN Australian/Canadian Osteoarthritis Hand Index, CRP C-reactive protein, ESR Erythrocyte sedimentation rate, NSAID Non-steroidal anti-inflammatory drug, OA Osteoarthritis. Joints according to ACR OA classification criteria were evaluated.