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Protocol for the first clinical trial to investigate safety and efficacy of corneal xenotransplantation in patients with corneal opacity, corneal perforation, or impending corneal perforation

机译:第一次临床试验的议定书,以研究角膜不透明度,角膜穿孔或即将发生角膜穿孔的患者角膜异种传导患者的安全性和疗效

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Background Xenotransplantation using fresh porcine corneas has been suggested as a feasible alternative to overcome the shortage of human donor corneas. Successful long-term survival of grafts without evidence of xenozoonosis in clinically applicable pig-to-non-human primate corneal transplantation model has brought researchers close to human clinical trials. Accordingly, we aimed to prepare a clinical trial protocol to conduct the first corneal xenotransplantation. Methods We developed the clinical trial protocol based on international consensus statement on conditions for undertaking clinical trials of corneal xenotransplantation developed by the International Xenotransplantation Society. Detailed contents of the protocol have been modified with reference to comments provided by ophthalmologists and multidisciplinary experts, including an infectionist, an organ transplantation specialist, a clinical pharmacologist, a neuropsychiatrist, a laboratory medicine doctor, and a microbiologist. Results Two patients with bilateral legal corneal blindness (best-corrected visual acuity = 20/200 in the better eye and = 20/1000 in the candidate eye) or with (impending) corneal perforation will be enrolled. During the screening period, participants and their family members will have two separate deep consideration periods before signing informed consent forms. Each patient will undergo corneal xenotransplantation using fresh corneas from Seoul National University miniature pigs. Commercially available immunosuppressants will be administered and systemic infection prophylaxis will be performed according to the program schedule. After transplantation, each patient will be monitored at a specialized clinic to investigate safety up to 2 years and efficacy up to 1 year. Conclusions A detailed clinical trial protocol for the first corneal xenotransplantation reflecting the global guidelines is provided.
机译:使用新鲜猪角膜的背景卵黄素被认为是克服人类供体玉米饼短缺的可行替代品。在没有临床上的猪对非人类动物激发模型的情况下,没有证据表明患有仇指鼻喉症的成功的长期存活,使研究人员接近人类临床试验。因此,我们旨在制备临床试验方案来进行第一个角膜异种传导。方法采用国际异常持近社会制定的临床试验的临床试验,开发了临床试验案例。通过参考眼科医生和多学科专家提供的评论进行了修改了议定书的详细内容,包括感染者,器官移植专家,临床药剂师,神经精神科医生,实验室医学博士和微生物学家。结果两名双侧法律角膜盲(最佳矫正敏锐度患者(在候选人眼中的更好的眼睛和& = 20/1000中)或候选人的眼球穿孔(即将发生)。在筛选期间,参与者及其家庭成员将在签署知情同意书之前有两个独立的深度考虑期。每位患者将使用来自首尔国立大学微型猪的新鲜玉米体进行角膜异叶植物。将施用市售免疫抑制剂,并根据方案时间表进行全身感染预防。移植后,将在专门的诊所监测每位患者,以调查安全长达2年,疗效长达1年。结论提供了反映全球准则的第一个角膜异种传道的详细临床试验方案。

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