首页> 外文期刊>Trials >A phase III, multi-centre, double-masked randomised controlled trial of adjunctive intraocular and peri-ocular steroid (triamcinolone acetonide) versus standard treatment in eyes undergoing vitreoretinal surgery for open globe trauma (ASCOT): statistical analysis plan
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A phase III, multi-centre, double-masked randomised controlled trial of adjunctive intraocular and peri-ocular steroid (triamcinolone acetonide) versus standard treatment in eyes undergoing vitreoretinal surgery for open globe trauma (ASCOT): statistical analysis plan

机译:眼内和眼周类固醇(醋酸曲安奈德)辅助类药物与标准治疗玻璃体视网膜手术治疗开放性眼球外伤(ASCOT)的III期,多中心,双盲,随机对照试验

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Background Open globe ocular trauma complicated by intraocular scarring (proliferative vitreoretinopathy) is a relatively rare, blinding, but potentially treatable condition for which, at present, surgery is often unsatisfactory and visual results frequently poor. To date, no pharmacological adjuncts to surgery have been proven to be effective. The aim of the Adjunctive Steroid Combination in Ocular Trauma (ASCOT) randomised controlled trial is to determine whether adjunctive steroid (triamcinolone acetonide), given at the time of surgery, can improve the outcome of vitreoretinal surgery in patients with open globe ocular trauma. This article presents the statistical analysis plan for the main publication as approved and signed off by the Trial Steering Committee prior to the first data extraction for the Data Monitoring Committee meeting report. Methods/design ASCOT is a pragmatic, multi-centre, parallel-group, double-masked randomised controlled trial. The aim of the study is to recruit from 20–25 centres in the United Kingdom and randomise 300 eyes (from 300 patients) into two treatment arms. Both groups will receive standard surgical treatment and care; the intervention arm will additionally receive a pre-operative steroid combination (triamcinolone acetonide) into the vitreous cavity consisting of 4 mg/0.1 ml and 40 mg/1 ml sub-Tenon’s. Participants will be followed for 6 months post-surgery. The primary outcome is the proportion of patients achieving a clinically meaning improvement in visual acuity in the study eye at 6 months after initial surgery, defined as a 10 letter score improvement in the ETDRS (the standard scale to test visual acuity). Trial registration ISRCTN30012492 . Registered on 5 September 2014. EudraCT2014-002193-37 . Registered on 5 September 2014.
机译:背景技术并发眼内瘢痕形成(增生性玻璃体视网膜病变)的开放性眼球外伤是一种相对罕见,致盲但可治疗的疾病,目前,该疾病的手术效果通常不理想,视觉效果也较差。迄今为止,尚无手术药理学辅助手段被证明是有效的。眼外伤辅助类固醇联合(ASCOT)随机对照试验的目的是确定手术时给予的辅助性类固醇(曲安奈德)可以改善玻璃体视网膜手术在开放性眼球外伤患者中的疗效。本文介绍了在数据监控委员会会议报告的首次数据提取之前,由试验指导委员会批准并签字的主要出版物的统计分析计划。方法/设计ASCOT是一项实用,多中心,平行分组,双掩蔽的随机对照试验。该研究的目的是从英国的20–25个中心招募人员,并将300只眼(来自300例患者)随机分为两个治疗组。两组都将接受标准的手术治疗和护理;介入臂还将在玻璃体腔中接受术前类固醇组合(曲安奈德),其中包括4 mg / 0.1 ml和40 mg / 1 ml的Tenon亚种。术后将对参与者进行6个月的随访。主要结局是在初次手术后6个月,研究眼的临床视力达到临床意义的患者比例,这被定义为ETDRS(测试视力的标准评分)提高了10个字母。试用注册ISRCTN30012492。 2014年9月5日注册。EudraCT2014-002193-37。 2014年9月5日注册。

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