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Safety and efficacy of compound methyl salicylate liniment for topical pain: A multicenter real-world study in China

Compound methyl salicylate liniment (Ammeltz) is composed of various components, such as methyl salicylate, menthol, camphor, chlorpheniramine maleate, and thymol. It was approved for listing in China in 2011. The purpose of this phase Ⅳ clinical trial was to evaluate the safety and efficacy of Amme...

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Autores principales: Guo, Jie, Hu, Xiaolei, Wang, Jing, Yu, Bin, Li, Juan, Chen, Jianting, Nie, Xiaoli, Zheng, Zhijian, Wang, Shixuan, Qin, Qun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9634125/
https://www.ncbi.nlm.nih.gov/pubmed/36339533
http://dx.doi.org/10.3389/fphar.2022.1015941
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author Guo, Jie
Hu, Xiaolei
Wang, Jing
Yu, Bin
Li, Juan
Chen, Jianting
Nie, Xiaoli
Zheng, Zhijian
Wang, Shixuan
Qin, Qun
author_facet Guo, Jie
Hu, Xiaolei
Wang, Jing
Yu, Bin
Li, Juan
Chen, Jianting
Nie, Xiaoli
Zheng, Zhijian
Wang, Shixuan
Qin, Qun
author_sort Guo, Jie
collection PubMed
description Compound methyl salicylate liniment (Ammeltz) is composed of various components, such as methyl salicylate, menthol, camphor, chlorpheniramine maleate, and thymol. It was approved for listing in China in 2011. The purpose of this phase Ⅳ clinical trial was to evaluate the safety and efficacy of Ammeltz in a real-life environment in China. Adverse events and adverse drug reactions were used to assess the safety of the monitored drugs. Visual analog scale (VAS) scores were evaluated to assess the severity of pain and the pain relief rate was used to evaluate the efficacy of the study drug. Of 3,600 subjects enrolled, 3,515 (97.64%) subjects completed the study and 85 (2.36%) terminated the study prematurely. A total of 277 adverse events occurred in 258 subjects (7.28%). The most common adverse events included upper respiratory infections (130 cases, 3.67%), local pruritus (17 cases, 0.48%), and diarrhea (12 cases, 0.34%). A total of 50 (1.41%) subjects experienced 58 adverse drug reactions. The most common adverse drug reactions included local pruritus (17 cases, 0.48%), a burning sensation at the application site (10 cases, 0.28%), and irritation at the application site (local) (7 cases, 0.2%). No adverse reactions were identified as new adverse drug reactions. The majority of adverse drug reactions were mild (48 cases, 1.36%), and no severe adverse drug reactions occurred. The subjects experienced significant pain relief after using Ammeltz (mean VAS scores: 5.34 vs. 2.79; Day 7 ± 1 vs. Baseline; p < 0.0001). The pain relief rate was 47.11% ± 23.13%, and in 2,769 cases (78.31%) the drug was effective in pain relief. After excluding subjects who used drugs that could affect the efficacy of the study drug, the subgroups of subjects experienced significant pain relief after using Ammeltz (mean VAS scores: 5.31 vs 2.77; Day 7 ± 1 vs Baseline; p < 0.0001). The pain relief rate was 47.34% ± 23.00%, and 2,612 subjects (78.75%) experienced effective pain relief. In conclusion, Ammeltz is safe and effective in real-life use. It can significantly relieve soft tissue pain caused by shoulder and neck pain, back pain, or muscle pain. No new adverse drug reactions were found in our multicenter real-world study. Clinical Trial Registration: https://clinicaltrials.gov/ct2/show/NCT05489939?cond=Safety+and+efficacy+of+compound+methyl+salicylate+liniment+for+topical+pain%3A+A+multicenter+real-world+study+in+China&draw=2&rank=1, identifier NCT05489939
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spelling pubmed-96341252022-11-05 Safety and efficacy of compound methyl salicylate liniment for topical pain: A multicenter real-world study in China Guo, Jie Hu, Xiaolei Wang, Jing Yu, Bin Li, Juan Chen, Jianting Nie, Xiaoli Zheng, Zhijian Wang, Shixuan Qin, Qun Front Pharmacol Pharmacology Compound methyl salicylate liniment (Ammeltz) is composed of various components, such as methyl salicylate, menthol, camphor, chlorpheniramine maleate, and thymol. It was approved for listing in China in 2011. The purpose of this phase Ⅳ clinical trial was to evaluate the safety and efficacy of Ammeltz in a real-life environment in China. Adverse events and adverse drug reactions were used to assess the safety of the monitored drugs. Visual analog scale (VAS) scores were evaluated to assess the severity of pain and the pain relief rate was used to evaluate the efficacy of the study drug. Of 3,600 subjects enrolled, 3,515 (97.64%) subjects completed the study and 85 (2.36%) terminated the study prematurely. A total of 277 adverse events occurred in 258 subjects (7.28%). The most common adverse events included upper respiratory infections (130 cases, 3.67%), local pruritus (17 cases, 0.48%), and diarrhea (12 cases, 0.34%). A total of 50 (1.41%) subjects experienced 58 adverse drug reactions. The most common adverse drug reactions included local pruritus (17 cases, 0.48%), a burning sensation at the application site (10 cases, 0.28%), and irritation at the application site (local) (7 cases, 0.2%). No adverse reactions were identified as new adverse drug reactions. The majority of adverse drug reactions were mild (48 cases, 1.36%), and no severe adverse drug reactions occurred. The subjects experienced significant pain relief after using Ammeltz (mean VAS scores: 5.34 vs. 2.79; Day 7 ± 1 vs. Baseline; p < 0.0001). The pain relief rate was 47.11% ± 23.13%, and in 2,769 cases (78.31%) the drug was effective in pain relief. After excluding subjects who used drugs that could affect the efficacy of the study drug, the subgroups of subjects experienced significant pain relief after using Ammeltz (mean VAS scores: 5.31 vs 2.77; Day 7 ± 1 vs Baseline; p < 0.0001). The pain relief rate was 47.34% ± 23.00%, and 2,612 subjects (78.75%) experienced effective pain relief. In conclusion, Ammeltz is safe and effective in real-life use. It can significantly relieve soft tissue pain caused by shoulder and neck pain, back pain, or muscle pain. No new adverse drug reactions were found in our multicenter real-world study. Clinical Trial Registration: https://clinicaltrials.gov/ct2/show/NCT05489939?cond=Safety+and+efficacy+of+compound+methyl+salicylate+liniment+for+topical+pain%3A+A+multicenter+real-world+study+in+China&draw=2&rank=1, identifier NCT05489939 Frontiers Media S.A. 2022-10-21 /pmc/articles/PMC9634125/ /pubmed/36339533 http://dx.doi.org/10.3389/fphar.2022.1015941 Text en Copyright © 2022 Guo, Hu, Wang, Yu, Li, Chen, Nie, Zheng, Wang and Qin. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pharmacology
Guo, Jie
Hu, Xiaolei
Wang, Jing
Yu, Bin
Li, Juan
Chen, Jianting
Nie, Xiaoli
Zheng, Zhijian
Wang, Shixuan
Qin, Qun
Safety and efficacy of compound methyl salicylate liniment for topical pain: A multicenter real-world study in China
title Safety and efficacy of compound methyl salicylate liniment for topical pain: A multicenter real-world study in China
title_full Safety and efficacy of compound methyl salicylate liniment for topical pain: A multicenter real-world study in China
title_fullStr Safety and efficacy of compound methyl salicylate liniment for topical pain: A multicenter real-world study in China
title_full_unstemmed Safety and efficacy of compound methyl salicylate liniment for topical pain: A multicenter real-world study in China
title_short Safety and efficacy of compound methyl salicylate liniment for topical pain: A multicenter real-world study in China
title_sort safety and efficacy of compound methyl salicylate liniment for topical pain: a multicenter real-world study in china
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9634125/
https://www.ncbi.nlm.nih.gov/pubmed/36339533
http://dx.doi.org/10.3389/fphar.2022.1015941
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