Table 5

Adverse events related to device or procedure in SIJF group (n = 102 subjects).

Event TypeN (%)*
Finding**
Fracture
Neuropathy
Pain
Post-operative***
Wound
Total		2 (2%)
1 (1%)
1 (1%)
9 (9%)
4 (4%)
5 (5%)
22 (23%)

  • ↵* Percent reported as number of events divided by number assigned to treatment

  • ↵** Physical examination or radiographic finding

  • ↵*** Postoperative issue, such as urinary retention, nausea/vomiting, atrial fibrillation.