Table I. —Adverse events throughout the study in the two groups.
Parameters | SWD group (N.=27) |
Control group (N.=13) |
P value |
---|---|---|---|
Overall, N. (%) | 2 (7.4) | 1 (7.7) | 1.000 |
Pulmonary fibrosis | 0 | 0 | |
Chest pain | 0 | 0 | |
Cardiac arrhythmia | 0 | 0 | |
Headache | 1 (3.7) | 1 (7.7) | |
Dizziness | 1 (3.7) | 0 | |
Burns | 0 | 0 |
Data are number of events (%). Patients with multiple events are counted once in each row.