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. 2016 May;39(3):272–280. doi: 10.1080/10790268.2015.1114224

Table 1.

Baseline characteristics of 64 patients with acute traumatic spinal cord injury who received progesterone and vitamin D or placebo

Progesterone + Vitamin D (n = 32) Placebo (n = 32) P-value
Age (years) 41.88 ± 13.6 45.2 ± 13.7 0.341
Sex
 Male (%) 19 (56.2%) 16 (50.0%) 0.802
 Female (%) 14 (43.8%) 16 (50.0%)
Injury Severity Score 28.9 ± 8.9 30.6 ± 9.4 0.224
Time between injury and intervention (hr) 3.62 ± 1.75 3.53 ± 1.83 0.835
 ≤4 hours 23 (71.9%) 22 (68.7%) 0.609
 >4 hours 9 (28.1%) 10 (31.3%)
Fracture site
 Cervical 7 (21.9%) 6 (18.8%) 0.652
  C4 (%) 3 (9.4%) 0 (0.0%)
  C5 (%) 0 (0.0%) 3 (9.4%)
  C6 (%) 4 (12.5%) 0 (0.0%)
  C7 (%) 0 (0.0%) 3 (9.4%)
 Thoracic 19 (59.5%) 19 (59.5%) 0.998
  T1 (%) 0 (0.0%) 3 (9.4%)
  T2 (%) 3 (9.4%) 0 (0.0%)
  T4 (%) 2 (6.2%) 3 (9.4%)
  T5 (%) 0 (0.0%) 4 (12.5%)
  T6 (%) 3 (9.4%) 0 (0.0%)
  T11 (%) 3 (9.4%) 6 (18.8%)
  T12 (%) 8 (25.0%) 3 (9.4%)
 Lumbar 6 (18.8%) 7 (21.9%) 0.652
  L1 (%) 6 (18.8%) 4 (12.5%)
  L2 (%) 0 (0.0%) 3 (9.4%)
Treatment
 Surgery (%) 12 (37.5%) 10 (31.2%) 0.793
 Conservative (%) 20 (62.5%) 22 (68.8%)