4.4 Article

Randomized Sham-controlled Double-Blind Multicenter Clinical Trial to Ascertain the Effect of Percutaneous Radiofrequency Treatment for Sacroiliac Joint Pain: Three-month Results

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CLINICAL JOURNAL OF PAIN
卷 32, 期 11, 页码 921-926

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LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/AJP.0000000000000351

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sacroiliac joint; radiofrequency; RCT; sham; chronic pain

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Objectives:To investigate the effect of a percutaneous radiofrequency (RF) heat lesion compared with a sham procedure, applied to the lateral branches of L5, S1, S2, S3, and S4 nerve roots.Materials and Methods:Sixty patients aged 18 years and above with a medical history and physical examination suggestive for sacroiliac joint pain and a reduction of 2 or more on a numerical rating scale (NRS, 0 to 10) after a sacroiliac joint test block were included in this study. Treatment group: percutaneous RF heat lesion at the lateral branches of S1, S2, S3, and S4 nerve roots and the posterior ramus dorsalis of L5; sham group: same procedure as the treatment group except for the RF heat lesion. Primary outcome measure: pain reduction (NRS). Secondary outcome measure: Global Perceived Effect.Results:No statistically significant differences in pain level over time between the groups (GroupxPeriod) (F-1,F-58=0.353; P=0.56) nor within the treatment Group (F-1,F-58=0.212; P=0.65) were found. The Period factor, however, yielded a significant difference (F-1,F-58=61.67; P<0.001), that is, when pooled together the mean pain level of the patients was significantly reduced at T1 compared with T0. In the crossover group, 42.1% experienced a reduction in NRS of 2 or more at 1 month (P=0.65). No statistically significant difference in satisfaction over time between the groups was found (F-1,F-50=2.1; P=0.15). The independent factors Group (F-1,F-50=2.02; P=0.16) and Period (F-1,F-50=0.95; P=0.33) also showed no statistically significant difference. The same applies to recovery: no statistically significant GroupxPeriod effect (F-1,F-51=0.09; P=0.77) was found, neither an effect of Group (F-1,F-51=0.004; P=0.95) nor of Period (F-1,F-51=0.27; P=0.60).Discussion:The hypothesis of no difference in pain reduction or in Global Perceived Effect between the treatment and sham group cannot be rejected.Level of Evidence:Level 1A.

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