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Safety and efficacy of clonazepam in patients with hemifacial spasm: A double-blind, randomized, placebo-controlled trial

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Authors

Baek, Seol-Hee; Shin, Je-Young; Sohn, Sung-Yeon; Park, Kee Hong; Kim, Jun-Soon; Kim, Bongjae; Ahn, So Hyun; Choi, Kyomin; Hong, Yoon-Ho; Sung, Jung-Joon

Issue Date
2022-10
Publisher
Elsevier BV
Citation
Parkinsonism and Related Disorders, Vol.103, pp.1-6
Abstract
© 2022 Elsevier LtdIntroduction: Hemifacial spasm (HFS) is an involuntary intermittent twitching of the facial muscles. Medical and surgical treatments can be considered for HFS. Among medical treatments, clonazepam is a benzodiazepine used to treat epilepsy, psychiatric symptoms, and movement disorders. This study aimed to investigate the efficacy and safety of clonazepam for the treatment of HFS. Methods: This randomized double-blind placebo-controlled trial prospectively enrolled patients with HFS aged 20–79 years. The patients were randomly assigned in a 1:1 ratio to receive either clonazepam (0.5 mg twice daily) or a placebo for 4 weeks. All participants underwent clinical assessment and laboratory tests at baseline and visit 2. The primary endpoint was the clinical global impression-improvement (CGI-I) score at visit 2. Results: A total of 34 patients with HFS assessed for eligibility were enrolled between April 2015 and November 2016. Among them, two patients were withdrawn before randomization. Thus, the intention-to-treat analysis included 32 patients with HFS. The median CGI-I scores at visit 2 did not differ significantly between the clonazepam (3; range 1–6) and placebo (3.5; range 3–5) groups. In the safety analysis, only mild or no serious adverse events were observed. Conclusion: The results of this study demonstrated the safety of clonazepam in patients with HFS. However, clonazepam did not show a statistically significant effect on HFS. Further studies are needed to provide evidence of the clinical benefits in patients with HFS.
ISSN
1353-8020
URI
https://hdl.handle.net/10371/185521
DOI
https://doi.org/10.1016/j.parkreldis.2022.07.025
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