Hashemi 2014.
Methods | Randomised controlled trial |
Participants |
Inclusion criteria
Exclusion criteria
|
Interventions | Group 1: pulsed RF using a 22 G cannula SMK C10 with method described by van Kleef et al applied for a duration of 120 s with 45 V with silent time 480 ms Group 2: steroid injections (1 mL (40 mg) triamcinolone) and 0.5 mL bupivacaine 0.5% |
Outcomes | Primary outcome: decrease in NRS score > 50% and pain relief defined as up to 6 months Secondary outcome: improvement in functional status (ODI) |
Notes |