Protocol for the RETHINK study: a randomised, double-blind, parallel-group, non-inferiority clinical trial comparing acetaminophen and NSAIDs for treatment of chronic pain in elderly patients with osteoarthritis of the hip and knee

被引:3
作者
Endo, Makoto [1 ]
Kawahara, Shinya [1 ]
Sato, Taishi [1 ]
Tokunaga, Masami [2 ]
Hara, Toshihiko [3 ]
Mawatari, Taro [4 ]
Kawano, Tsutomu [5 ]
Zenda, Sadamoto [6 ]
Miyaji, Tempei [7 ]
Shimokawa, Mototsugu [8 ]
Sakamoto, Sanae [9 ]
Takano, Toshio [10 ]
Miyake, Masumi [10 ]
Aono, Hiroyuki [10 ]
Nakashima, Yasuharu [1 ]
RETHINK Study Grp
机构
[1] Kyushu Univ, Dept Orthopaed Surg, Fukuoka, Japan
[2] Fukuoka Orthopaed Hosp, Dept Orthopaed Surg, Fukuoka, Japan
[3] Aso Iizuka Hosp, Dept Orthopaed Surg, Iizuka, Fukuoka, Japan
[4] Hamanomachi Hosp, Dept Orthopaed Surg, Fukuoka, Japan
[5] Kyushu Rosai Hosp, Dept Orthopaed Surg, Kitakyushu, Fukuoka, Japan
[6] Natl Canc Ctr Hosp East, Dept Radiat Oncol, Kashiwa, Chiba, Japan
[7] Univ Tokyo, Grad Sch Med, Dept Clin Trial Data Management, Tokyo, Japan
[8] Yamaguchi Univ, Dept Biostat, Grad Sch Med, Ube, Yamaguchi, Japan
[9] Fukuoka Data Ctr Clin Trials, Fukuoka, Japan
[10] Ayumi Pharmaceut Corp, Tokyo, Japan
来源
BMJ OPEN | 2023年 / 13卷 / 02期
关键词
pain management; orthopaedic & trauma surgery; EFFICACY; IBUPROFEN; PARACETAMOL; INVENTORY; CELECOXIB;
D O I
10.1136/bmjopen-2022-068220
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
IntroductionIn patients with chronic pain, oral analgesics are essential treatment options to manage pain appropriately, improve activities of daily living abilities and achieve a higher quality of life (QOL). It is desirable to select analgesics for elderly patients based on comparative data on analgesic effect and risk of adverse events; however, there are few comparative studies so far. The purpose of this study is to determine whether the efficacy and safety of acetaminophen are non-inferior to non-steroidal anti-inflammatory drugs (NSAIDs) in the treatment of chronic pain associated with osteoarthritis of the hip and knee in elderly patients.Methods and analysisThis study is a multicentre, randomised controlled, double-blind, parallel-group study to compare the analgesic effect and adverse events between acetaminophen or NSAIDs (loxoprofen or celecoxib). A total of 400 elderly patients with osteoarthritis of the hip and knee will be recruited from five institutions in Japan. Patients of 65 years or older with osteoarthritis-related pain will be registered and randomly assigned to acetaminophen, loxoprofen or celecoxib with 2:1:1 allocation. The primary endpoint is change in the Brief Pain Inventory (BPI) item 3 (worst pain) score from baseline to week 8. The secondary endpoints are BPI item 3 score change from baseline to week 4, health-related QOL measured by Short Form-8 Health Survey, and occurrence of adverse events including gastrointestinal disorders and abnormal liver function. Data will be analysed in accordance with a predefined statistical analysis plan.Ethics and disseminationThis study protocol was approved by the Kyushu University Hospital Certified Institutional Review Board for Clinical Trials on 28 January 2021 (KD2020004) and the chief executive of each participating hospital. The results of the study will be submitted to international peer-reviewed journals, and the main findings will be presented at international scientific conferences.
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页数:7
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