首页> 外文期刊>Clinical ophthalmology >A randomized double-masked study to compare the ocular safety, tolerability, and efficacy of bromfenac 0.075% compared with vehicle in cataract surgery subjects
【24h】

A randomized double-masked study to compare the ocular safety, tolerability, and efficacy of bromfenac 0.075% compared with vehicle in cataract surgery subjects

机译:在白内障手术对象中进行随机双盲研究,比较溴芬酸与赋形剂相比,眼用安全性,耐受性和功效为0.075%

获取原文
           

摘要

Purpose: The aim of this study was to evaluate the safety, tolerability, and efficacy of a low-dose version of bromfenac 0.075% in DuraSite? (bromfenac 0.075%) compared with DuraSite??vehicle (vehicle) alone for the treatment of postoperative inflammation and ocular pain after cataract surgery. Methods: A multicenter, double-masked, vehicle-controlled, parallel-group clinical trial of 240?subjects randomized in a 2:1 ratio to bromfenac 0.075% or vehicle was conducted. Subjects were dosed BID beginning 1?day before the cataract surgery, the day of surgery, and 14?days after surgery. A slit lamp biomicroscopy examination was performed to evaluate the signs of inflammation, including anterior chamber cells (ACC) and anterior chamber flare (ACF). The primary efficacy variable was the proportion of subjects with an ACC grade of 0 at Day 15. Secondary efficacy endpoints included the proportion of subjects who achieved a pain score of 0 at each postsurgical visual analog scale (VAS) assessment and the proportion of subjects with an ACF grade of 0 at Day 15. Results: At Day 15, proportionally more subjects in the bromfenac 0.075% group than in the vehicle group had an ACC grade of 0 (57.1% vs 18.8%, respectively; P <0.001). At?each of the postsurgical time points (Days 1, 8, 15, and 29), proportionally more bromfenac 0.075%-treated subjects (76.8%, 90.5%, 92.9%, and 85.1%, respectively) had no pain (a VAS score of 0) compared with the vehicle-treated subjects (48.2%, 38.8%, 42.4%, and 47.1%, respectively), and at each time point, these differences in proportions were statistically significant ( P <0.001). More subjects in the bromfenac 0.075% group had complete ACF resolution (151/167; 90.4%) compared to those in the vehicle group (54/85; 63.5%). There were no new safety signals reported. Conclusion: Bromfenac 0.075% in DuraSite is safe, well tolerated, and effective at reducing inflammation and preventing pain associated with cataract surgery.
机译:目的:本研究的目的是评估与DuraSite ?相比,DuraSite ?(bromfenac 0.075%)中低剂量版本的溴芬酸(0.075%)的安全性,耐受性和疗效。单独使用的车辆(车辆)用于治疗白内障手术后的术后炎症和眼痛。方法:进行了一项多中心,双掩蔽,媒介物控制的平行组临床试验,以240:1的受试者以0.01%的溴芬酸或媒介物的比例随机分配为2:1。在白内障手术前1天,手术当天和手术后14天开始给受试者BID剂量。进行裂隙灯生物显微镜检查以评估炎症迹象,包括前房细胞(ACC)和前房耀斑(ACF)。主要功效变量是在第15天ACC等级为0的受试者的比例。次要功效终点包括在每次术后视觉模拟量表(VAS)评估中达到疼痛评分为0的受试者的比例以及第15天的ACF等级为0。结果:在第15天,溴芬酸0.075%组的受试者ACC等级为0的比例更高(分别为57.1%对18.8%; P <0.001)。在每个术后时间点(第1、8、15和29天),按比例接受0.075%溴芬酸治疗的受试者(分别为76.8%,90.5%,92.9%和85.1%)没有疼痛(VAS)与接受车辆治疗的受试者(分别为48.2%,38.8%,42.4%和47.1%)相比,得分为0),并且在每个时间点,这些比例的差异均有统计学意义(P <0.001)。相比于媒介物组(54/85; 63.5%),溴芬酸0.075%组中更多的受试者具有完全的ACF分辨率(151/167; 90.4%)。没有新的安全信号报告。结论:DuraSite中的溴芬酸0.075%安全,耐受性良好,可有效减少白内障手术引起的炎症和预防疼痛。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号