Aravind Eye Hospital, Madurai, India.
Federal University of São Paulo, São Paulo, Brazil.
Trials. 2024 Aug 28;25(1):566. doi: 10.1186/s13063-024-08376-3.
Infectious keratitis secondary to fungus or acanthamoeba often has a poor outcome despite receiving the best available medical therapy. In vitro rose bengal photodynamic therapy (RB-PDT) appears to be effective against fungal and acanthamoeba isolates (Atalay HT et al., Curr Eye Res 43:1322-5, 2018, Arboleda A et al. Am J Ophthalmol 158:64-70, 2014). In one published series, RB-PDT reduced the need for therapeutic penetrating keratoplasty in severe bacterial, fungal, and acanthamoeba keratitis not responsive to medical therapy.
This international, randomized, sham and placebo controlled 2-arm clinical trial randomizes patients with smear positive fungal and acanthamoeba and smear negative corneal ulcers in a 1:1 fashion to one of two treatment arms: 1) topical antimicrobial plus sham RB-PDT or 2) topical antimicrobial plus RB-PDT.
We anticipate that RB-PDT will improve best spectacle-corrected visual acuity and also reduce complications such as corneal perforation and the need for therapeutic penetrating keratoplasty. This study will comply with the NIH Data Sharing Policy and Policy on the Dissemination of NIH-Funded Clinical Trial Information and the Clinical Trials Registration and Results Information Submission rule. Our results will be disseminated via ClinicalTrials.gov website, meetings, and journal publications. Our data will also be available upon reasonable request.
NCT, NCT05110001 , Registered on November 5, 2021.
真菌感染或棘阿米巴感染引起的感染性角膜炎,即使接受了最佳的药物治疗,其预后仍较差。体外孟加拉玫瑰红光动力疗法(RB-PDT)似乎对真菌和棘阿米巴分离株有效(Atalay HT 等人,Curr Eye Res 43:1322-5,2018;Arboleda A 等人,Am J Ophthalmol 158:64-70,2014)。在一项已发表的研究中,RB-PDT 减少了对药物治疗无反应的严重细菌性、真菌性和棘阿米巴性角膜炎患者对治疗性穿透性角膜移植术的需求。
本研究为国际、随机、假对照和安慰剂对照的 2 臂临床试验,以 1:1 的比例将涂片阳性的真菌和棘阿米巴以及涂片阴性的角膜溃疡患者随机分配到以下两个治疗组之一:1)局部抗菌药联合假 RB-PDT 或 2)局部抗菌药联合 RB-PDT。
我们预计 RB-PDT 将改善最佳矫正视力,并减少角膜穿孔和治疗性穿透性角膜移植术的需求等并发症。本研究将符合 NIH 数据共享政策和 NIH 资助的临床试验信息传播政策以及临床试验注册和结果信息提交规则。我们的研究结果将通过 ClinicalTrials.gov 网站、会议和期刊出版物进行传播。应合理要求,我们的数据也将提供。
NCT05110001,于 2021 年 11 月 5 日注册。