Skip to main content

Table 2 Baseline demographic and clinical variables of the Traumeel S® and placebo treatment groups.

From: Traumeel S® for pain relief following hallux valgus surgery: a randomized controlled trial

 

Traumeel S®

(n = 39)

Placebo

(n = 40)

Clinical Center:

  

   SZMC*

33

34

   MMC**

6

6

Age (y)

  

   Mean (SD)

48.1 (16.7)

45.2 (18.7)

   < 50

17

19

   ≥ 50

22

21

Sex (%)

  

   M

8 (20.5)

8 (20.0)

   F

31 (79.5)

32 (80.0)

Ethnicity/Origin (%)

  

   Europe/America

12 (30.8)

9 (22.5)

   Asia/Africa

21 (53.9)

25 (62.5)

   Israeli Arab

2 (5.1)

0

   Mixed

2 (5.1)

2 (5.0)

   Other

2 (5.1)

4 (10.0)

BMI

  

   Mean (SD)

24.7 (4.1)

24.3 (4.0)

   < 24

20

23

   ≥ 24

18

16

Pain before surgery

  

   Mean (SD)

5.4 (2.8)

5.7 (2.6)

   < 6

19

18

   ≥ 6

20

21

Laterality (%)

  

   Right

21 (53.9)

14 (35.9)

   Left

16 (41.0)

24 (61.5)

   Bilateral#

2 (5.1)

1 (2.6)

Type of surgery (%)

  

   Chevron - only

9 (23.0)

10†† (26.3)

   Additional

17 (43.5)

18 (47.3)

   osteotomy

  

   Triple or

13 (33.3)

10 (26.3)

   proximal

  

   osteotomy

  
  1. * SZMC -- Shaare Zedek Medical Center
  2. **MMC -- Meir Medical Center
  3. #3 patients had a bilateral hallux valgus but underwent surgery on only one foot.
  4. - includes 1 patient with missing data.
  5. ††-includes 2 patients with missing data.