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REKOVER 研究方案:亚洲真实世界环境中曲马多和右旋酮洛芬氨丁三醇口服用固定剂量复方制剂(SKUDEXA)治疗中度至重度急性疼痛的前瞻性患者治疗登记研究。

REKOVER study protocol: a pRospective patient treatment rEgistry of tramadol and dexKetoprofen trometamol oral fixed-dose combination (SKUDEXA) in mOderate to seVere acutE pain in Real-world setting in Asia.

机构信息

The Pain Clinic, Mount Alvernia Medical Centre, Singapore

Medical Affairs, A Menarini Asia Pacific Holdings Pte Ltd, Singapore.

出版信息

BMJ Open. 2024 Mar 19;14(3):e080620. doi: 10.1136/bmjopen-2023-080620.

Abstract

INTRODUCTION

Satisfactory management of acute pain remains a major medical challenge despite the availability of multiple therapeutic options including the fixed-dose combination (FDC) drugs. Tramadol and dexketoprofen trometamol (TRAM/DKP) 75/25 mg FDC was launched in 2018 in Asia and is widely used in the management of moderate to severe acute pain. There are limited data on its effectiveness and safety in Asian patients, and therefore, a need to better understand its usage patterns in clinical practice. We aim to understand the usage pattern of TRAM/DKP FDC, its effectiveness and tolerability in patients with moderate to severe acute pain in Asia.

METHODS AND ANALYSIS

REKOVER is a phase-IV, multicountry, multicentre, prospective, real-world observational study. A total of 750 postsurgical and non-surgical patients (male and female, aged 18-80 years) will be recruited from 13 tertiary-care hospitals (15 sites) in Singapore, Thailand, the Philippines and Malaysia. All patients prescribed with TRAM/DKP FDC and willing to participate in the study will be enrolled. The recruitment duration for each site will be 6 months. The severity of pain will be collected using Numeric Pain Rating Scale through the treatment period from day 1 to day 5, while satisfaction with the treatment will be evaluated using Patient Global Evaluation Scale at the end of treatment. Any adverse event reported during the study duration will be recorded for safety analysis (up to day 6). The study data will be entered into the ClaimIt portal and mobile application (app) (ObvioHealth, USA). All the inpatient data will be entered into the portal by the study site and for outpatient it will be done by patients through an app.

ETHICS AND DISSEMINATION

The study has been approved by the local ethics committee from each study sites in Singapore, Thailand, the Philippines and Malaysia. Findings will be disseminated through local and global conference presentations, publications in peer-reviewed scientific journals and continuing medical education.

摘要

简介

尽管有多种治疗选择,包括固定剂量组合(FDC)药物,但急性疼痛的满意管理仍然是一个主要的医学挑战。曲马多和右旋酮洛芬托美丁(TRAM/DKP)75/25mg FDC 于 2018 年在亚洲推出,广泛用于治疗中重度急性疼痛。亚洲患者中关于其有效性和安全性的数据有限,因此需要更好地了解其在临床实践中的使用模式。我们旨在了解亚洲中重度急性疼痛患者使用 TRAM/DKP FDC 的模式、其疗效和耐受性。

方法和分析

REKOVER 是一项四期、多国家、多中心、前瞻性、真实世界观察研究。将从新加坡、泰国、菲律宾和马来西亚的 13 家三级保健医院(15 个地点)招募总共 750 名术后和非手术患者(男性和女性,年龄 18-80 岁)。所有开处方 TRAM/DKP FDC 并愿意参与研究的患者将被纳入研究。每个地点的招募时间为 6 个月。治疗期间(第 1 天至第 5 天)将使用数字疼痛评分量表收集疼痛严重程度,治疗结束时将使用患者总体评价量表评估治疗满意度。在研究期间报告的任何不良事件都将进行安全性分析(最多至第 6 天)。研究数据将输入 ClaimIt 门户和移动应用程序(ObvioHealth,美国)。所有住院数据将由研究地点输入门户,对于门诊患者将由患者通过应用程序输入。

伦理和传播

该研究已获得新加坡、泰国、菲律宾和马来西亚每个研究地点的当地伦理委员会的批准。研究结果将通过当地和全球会议报告、同行评议科学期刊发表和继续医学教育进行传播。

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