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정형외과 수술 후 5일간 투여 된 로페콕시브 50mg의 진통효과 -치료약 대조, 무작위배정, 다기관, 공개 임상시험-
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  • 정형외과 수술 후 5일간 투여 된 로페콕시브 50mg의 진통효과 -치료약 대조, 무작위배정, 다기관, 공개 임상시험-
저자명
김정만,김희중,배대경,서재곤,선두훈,성상철,이명철,이수호,조우신,조윤제,한창동,이우석,김강일,안진환,이석현,박윤수,Kim. Jung-Man,Kim. Hee-Joong,Bae. Dae-Kyung,Seo. Jai-Gon,Sun. Do
간행물명
臨床藥理學會誌= The journal of Korean Society for Clinical Pharmacology and Therapeutics
권/호정보
2000년|8권 2호|pp.213-222 (10 pages)
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대한임상약리학회
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이 논문은 한국과학기술정보연구원과 논문 연계를 통해 무료로 제공되는 원문입니다.
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기타언어초록

Background: Nonsteroidal anti-inflammatory drugs(NSAIDs) inhibit both cyclooxygenase-1(COX1) and cyclooxygenase-2(COX-2). There have been several trials showing that a specific inhibitor of COX-2 provide efficacy in surgical pain comparable with NSAIDs. In this study, the efficacy and safety of the rofecoxib which specifically inhibits COX-2 were compared with aceclofenac, an NSAID, in patients with pain after orthopedic surgery. Method : A randomized, open, active comparator-controlled trial of 229 adults with orthopedic surgical pain was conducted. Patients were randomized to one of two treatment groups ; 50mg of rofecoxib once daily or 100mg of aceclofenac twice daily. Clinical efficacy and safety were evaluated over 5-day treatment period. Result : Rofecoxib at dosage of 50mg demonstrated efficacy that was clinically comparable to that of aceclofenac as assessed by primary endpoint(TOPAR8) according to predefined comparability criteria. Results from secondary endpoints(SPID8, patient global assessment of response to therapy) were consistent with those of the primary endpoint. All treatments were generally well tolerated. Conclusion : Rofecoxib was well tolerated and provided efficacy that was clinically comparable, according to predefined equivalence margin, to that of 100mg of aceclofenac twice daily in this 5-day study.