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. 2021 May 27;58(1):137–143. doi: 10.23736/S1973-9087.21.06892-1

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.