Table 5.
Studies concerning the use of botulinum toxin type A (BoNT-A) in notalgia paresthetica
| First author [Ref.], year | Type of study | n | BoNT-A doses | Retreatment | Follow-up | Results |
|---|---|---|---|---|---|---|
| Maari [72], 2014 | RCT vs. placebo double-blind | 20 | max 200 U | No | 12 weeks, then placebo arm shifted to BoNT-A; total 24 weeks | No significant difference for pruritus (VAS) and hyperpigmentation |
| Pèrez-Pèrez [73], 2014 | Retrospective, case series | 5 | 48 – 56 U | No | 18 months | 2 worsening pruritus, little improvement in other 3 but for only 1 month |
| Wallengren [71], 2010 | Prospective | 6 | 18 ' 100 U | No | 18 months | 5/6 patients a mean reduction of VAS by 28% at week 6; at 18 months 1 patient had a VAS of 45%, another one was still free from itch |
| Weinfeld [70], 2007 | Case report | 2 | 16 ' 24 U | Yes, 18 months later with 48 U (only 1 patient) | 18 months | Improvement (patient self-assessment) |
RCT, randomized clinical trial; VAS, Visual Analogue Scale.