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含双氯芬酸新型脂质凝胶的疗效与安全性评估:一项针对骨关节炎体征和症状患者的随机、安慰剂对照、双盲临床试验

Evaluation of efficacy and safety of a novel lipogel containing diclofenac: A randomized, placebo controlled, double-blind clinical trial in patients with signs and symptoms of osteoarthritis.

作者信息

Bhatia Amit, Goni Vijay, Chopra Shruti, Singh Bhupinder, Katare Om Prakash

机构信息

Department of Pharmaceutical Sciences and Technology, Maharaja Ranjit Singh Punjab Technical University, Badal Road, Bathinda, Punjab, 151 001, India.

Amity Institute of Pharmacy, Amity University, Sector 125, Noida, Uttar Pradesh, 201 303, India.

出版信息

Contemp Clin Trials Commun. 2020 Oct 7;20:100664. doi: 10.1016/j.conctc.2020.100664. eCollection 2020 Dec.

Abstract

BACKGROUND

Effectiveness and safety of pharmaceuticals is the prime concern of every osteoarthritis (OA) treatment. Chronic administration of NSAIDs, especially in case of geriatrics, through oral route tend to compromise the patient's safety, whereas topical treatments are not found to be effective owing their poor ability to deliver drug molecules.Thus, the present study deals with a randomized, double-blind, controlled trial conducted on patients with knee osteoarthritis (OA) for comparing the performance of a novel topical gel (liposomal gel) of diclofenac with a placebo and a marketed gel.

METHODS

The patients were treated and evaluated for 6 weeks as per the Western Ontario McMaster Universities (WOMAC) Index for OA. Patients were also observed for any adverse events. All the results were analyzed statistically using Kruskal-Wallis test, followed by Student's t-test at p ≤ 0.05.

RESULTS

Patients treated with liposomal gel showed statistically significantly improvements in treatment in comparison to the other tested formulations. All the treatments were found to be well tolerated with no report of adverse event. The results unequivocally demonstrated the superiority of the diclofenac liposomal gel, in the relieving the symptoms of OA of the knee, in comparison to placebo and marketed gel.

CONCLUSION

From above results it was revealed that the drug in liposome have higher therapeutic potential. Thus, this can be a safe and effective option for the management of chronic OA especially for geriatric patients.

摘要

背景

药物的有效性和安全性是每种骨关节炎(OA)治疗的首要关注点。非甾体抗炎药(NSAIDs)的长期口服给药,尤其是在老年患者中,往往会损害患者的安全性,而局部治疗由于其输送药物分子的能力较差而未被发现有效。因此,本研究针对膝骨关节炎(OA)患者进行了一项随机、双盲、对照试验,以比较双氯芬酸新型局部凝胶(脂质体凝胶)与安慰剂和市售凝胶的性能。

方法

根据西安大略麦克马斯特大学(WOMAC)骨关节炎指数对患者进行为期6周的治疗和评估。还观察患者是否有任何不良事件。所有结果均使用Kruskal-Wallis检验进行统计学分析,随后在p≤0.05时进行学生t检验。

结果

与其他测试制剂相比,用脂质体凝胶治疗的患者在治疗上显示出统计学上的显著改善。所有治疗均耐受性良好,未报告不良事件。结果明确表明,与安慰剂和市售凝胶相比,双氯芬酸脂质体凝胶在缓解膝骨关节炎症状方面具有优越性。

结论

从上述结果可以看出,脂质体中的药物具有更高的治疗潜力。因此,这对于慢性骨关节炎的管理,尤其是老年患者,可能是一种安全有效的选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/90a8/7593528/b4d06d2fcb31/fx1.jpg

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