Table 3.
Concomitant therapy administered and adverse events reported.
| Overall patients (n = 92) | Control Group (n = 44) | Blood Ozonization Group (n = 48) | P | |
|---|---|---|---|---|
| Concomitant therapy | ||||
|
87 (94.6%) | 42 (95.5%) | 45 (93.8%) | 1.000 |
|
92 (100%) | 44 (100%) | 48 (100%) | 1.000 |
|
56 (60.9%) | 32 (72.7%) | 24 (50.0%) | 0.044 |
|
68 (73.9%) | 31 (70.5%) | 37 (77.1%) | 0.627 |
|
43 (46.7%) | 20 (45.5%) | 23 (47.9%) | 0.978 |
|
5 (5.4%) | 1 (2.3%) | 4 (8.3%) | 0.412 |
| Adverse events | ||||
|
15 (16.3%) | 7 (16.3%) | 8 (16.7%) | 1.000 |
|
4 (4.4%) | 3 (6.8%) | 1 (2.1%) | 0.548 |
|
7 (7.6%) | 3 (6.8%) | 4 (8.3%) | 1.000 |
|
3 (3.3%) | 0 (0.0%) | 3 (6.3%) | 0.272 |
|
10 (10.9%) | 5 (11.4%) | 5 (10.4%) | 1.000 |
|
6 (6.5%) | 3 (6.8%) | 3 (6.3%) | 1.000 |