Efficacy and Safety of Aceclofenac-CR and Aceclofenac in the Treatment of Knee Osteoarthritis: A 6-Week, Comparative, Randomized, Multicentric, Double-Blind Study

被引:12
|
作者
Pareek, Anil [1 ]
Chandurkar, Nitin [1 ]
Gupta, Anil [2 ]
Sirsikar, Ashish [3 ,4 ]
Dalal, Bhavik [5 ,6 ]
Jesalpura, Bhavesh [7 ]
Mehrotra, Anoop [8 ,9 ]
Mukherjee, Arunangshu [10 ,11 ]
机构
[1] Ipca Labs Ltd, Med Affairs & Clin Res, Bombay 400067, Maharashtra, India
[2] Mahatma Gandhi Med Coll & Hosp, Dept Orthoped, Jaipur, Rajasthan, India
[3] GR Med Coll Hosp, Dept Orthoped, Gwalior, India
[4] JA Grp Hosp, Dept Orthoped, Gwalior, India
[5] Smt NHL Municipal Med Coll, Dept Orthopaed Surg, Ahmadabad, Gujarat, India
[6] SCL Municipal Gen Hosp, Dept Orthopaed Surg, Ahmadabad, Gujarat, India
[7] Sheth VS Hosp, Dept Orthoped, Ahmadabad, Gujarat, India
[8] Gandhi Med Coll, Dept Orthopaed, Bhopal, India
[9] Hamidia Hosp, Dept Orthopaed, Bhopal, India
[10] Mahatma Gandhi Mem Med Coll, Dept Orthopaed, Indore, India
[11] Maharaja Yashwantrao Hosp, Dept Orthopaed, Indore, India
来源
JOURNAL OF PAIN | 2011年 / 12卷 / 05期
关键词
Aceclofenac; control release; knee osteoarthritis; NSAIDs; MANAGEMENT; OUTCOMES; BURDEN; TRIAL; PAIN; HIP; MG;
D O I
10.1016/j.jpain.2010.10.013
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The efficacy and safety of aceclofenac control release (CR) tablets was compared with conventional aceclofenac tablets in patients with knee osteoarthritis (OA). This was a double-blind, double-dummy, randomized, parallel group multicentric study conducted at 6 centers. Two hundred and eighty five patients were randomized to either aceclofenac-CR (n = 143) once daily or conventional aceclofenac tablet (n = 142) twice daily and were followed for 6 weeks. The efficacy parameters were pain intensity score on visual analogue scale, Western Ontario and McMaster (WOMAC) score, patients and investigator's overall study drug assessment and total consumption of acetaminophen and ranitidine tablets. Both treatments showed significant improvement in their efficacy parameters from baseline at the end of therapy. Aceclofenac-CR was comparable to conventional aceclofenac with respect to change in pain intensity and WOMAC score (P > .05) There was no statistically significant difference between the treatment groups in patient's and investigator's overall study drug assessment at the end of therapy (P > .05). Aceclofenac-CR treated patients took fewer acetaminophen and ranitidine tablets during the treatment period as compared to conventional aceclofenac treated patients. Both the study medications were well tolerated with no incidence of serious adverse event (SAE). In conclusion, the new aceclofenac-CR formulation was found to be effective and safe while offering practical advantage of once daily administration. Perspective: This article represents the advantages of control release aceclofenac over the conventional aceclofenac tablets. Aceclofenac-CR was found to be similar in terms of efficacy as conventional aceclofenac in knee OA patients with fewer adverse events. (C) 2011 by the American Pain Society
引用
收藏
页码:546 / 553
页数:8
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