Polmacoxib 2mg in patients with mild to moderate idiopathic osteoarthritis of hip/knee-a randomized, double-anonymous study.

IF 1.4 Q4 CLINICAL NEUROLOGY
Pain management Pub Date : 2024-09-01 Epub Date: 2024-11-15 DOI:10.1080/17581869.2024.2427944
Shubhadeep D Sinha, Tadikonda Bhavani Prasad, Bhaskar Konatham, Sreenivasa Chary Sriramadasu, Arnab Karmakar, Arun Kumar Sharma, Rakesh Verma, Srinivas Reddy Devireddy, Mohan Reddy Bandi, Muralidhar Panapakam
{"title":"Polmacoxib 2mg in patients with mild to moderate idiopathic osteoarthritis of hip/knee-a randomized, double-anonymous study.","authors":"Shubhadeep D Sinha, Tadikonda Bhavani Prasad, Bhaskar Konatham, Sreenivasa Chary Sriramadasu, Arnab Karmakar, Arun Kumar Sharma, Rakesh Verma, Srinivas Reddy Devireddy, Mohan Reddy Bandi, Muralidhar Panapakam","doi":"10.1080/17581869.2024.2427944","DOIUrl":null,"url":null,"abstract":"<p><strong>Aim: </strong>Polmacoxib, a new COX-2 inhibitor with carbonic anhydrase (CA) inhibitory action, is expected to help minimize the adverse effects associated with other NSAIDs, like GI (gastrointestinal) and CV (cardiovascular) system- related issues. The comparative efficacy and safety of polmacoxib 2 mg (manufactured by Hetero Labs Limited) versus celecoxib 200 mg (manufactured by Hetero Labs Limited) were assessed in this randomized, double-anonymous, clinical study in Indian adult patients diagnosed with idiopathic osteoarthritis (OA) of the.</p><p><strong>Patients & methodology: </strong>18 years and older patients of either sex, clinically and radiographically diagnosed idiopathic knee or hip OA were randomized to receive either polmacoxib or celecoxib in a 1:1 ratio. All patients were assessed with various pain measuring scales and recorded the scores at the end of weeks 3 and 6.</p><p><strong>Conclusion: </strong>The data for all the pain assessment scores were analyzed, and polmacoxib was found to be a non-inferior therapeutic agent compared to celecoxib in terms of safety and efficacy.(https://ctri.nic.in/CTRI/2022/05/042923).</p>","PeriodicalId":20000,"journal":{"name":"Pain management","volume":" ","pages":"497-506"},"PeriodicalIF":1.4000,"publicationDate":"2024-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Pain management","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1080/17581869.2024.2427944","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/11/15 0:00:00","PubModel":"Epub","JCR":"Q4","JCRName":"CLINICAL NEUROLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Aim: Polmacoxib, a new COX-2 inhibitor with carbonic anhydrase (CA) inhibitory action, is expected to help minimize the adverse effects associated with other NSAIDs, like GI (gastrointestinal) and CV (cardiovascular) system- related issues. The comparative efficacy and safety of polmacoxib 2 mg (manufactured by Hetero Labs Limited) versus celecoxib 200 mg (manufactured by Hetero Labs Limited) were assessed in this randomized, double-anonymous, clinical study in Indian adult patients diagnosed with idiopathic osteoarthritis (OA) of the.

Patients & methodology: 18 years and older patients of either sex, clinically and radiographically diagnosed idiopathic knee or hip OA were randomized to receive either polmacoxib or celecoxib in a 1:1 ratio. All patients were assessed with various pain measuring scales and recorded the scores at the end of weeks 3 and 6.

Conclusion: The data for all the pain assessment scores were analyzed, and polmacoxib was found to be a non-inferior therapeutic agent compared to celecoxib in terms of safety and efficacy.(https://ctri.nic.in/CTRI/2022/05/042923).

针对轻度至中度特发性髋关节/膝关节骨关节炎患者的 2 毫克波马昔布--一项随机、双匿名研究。
目的:波马昔布是一种具有碳酸酐酶(CA)抑制作用的新型COX-2抑制剂,有望帮助减少与其他非甾体抗炎药相关的不良反应,如与胃肠道和心血管系统相关的问题。在这项随机、双匿名临床研究中,对被诊断为特发性骨关节炎(OA)的印度成年患者进行了波马昔布 2 毫克(由 Hetero Labs Limited 生产)与塞来昔布 200 毫克(由 Hetero Labs Limited 生产)的疗效和安全性对比评估。患者和方法:18 岁及以上经临床和影像学诊断为特发性膝关节或髋关节 OA 的男女患者按 1:1 的比例随机接受波马昔布或塞来昔布治疗。所有患者均接受了各种疼痛测量量表的评估,并在第3周和第6周结束时记录了评分:对所有疼痛评估评分数据进行分析后发现,就安全性和有效性而言,波马昔布的治疗效果不优于塞来昔布。(https://ctri.nic.in/CTRI/2022/05/042923)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Pain management
Pain management CLINICAL NEUROLOGY-
CiteScore
2.90
自引率
5.90%
发文量
62
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信