跳至主要内容
临床试验/ISRCTN85921622
ISRCTN85921622已完成未知

A novel, high-definition PERSONALised artificial EYE Service (PERSONAL-EYE-S): a cross-over, randomised feasibility study of digitally printed versus hand-painted artificial eyes in adults

eeds Teaching Hospitals NHS Trust0 个研究点目标入组 35 人开始时间: 2021年6月17日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
发起方
入组人数
35

研究概览

简要总结

2023 Protocol article in https://pubmed.ncbi.nlm.nih.gov/37056714/ (added 17/04/2023) 2024 Results article in https://pubmed.ncbi.nlm.nih.gov/39095468/ (added 06/08/2024)

研究设计

研究类型
Interventional

入排标准

性别
All

入选标准

  • 1. Aged =18 years
  • 2. Longstanding artificial eye user (at least 12 months post-operation)
  • 3. Requires a replacement artificial eye (can be due to a variety of reasons such as wear and tear; damage; loss, change in fitting, clinician opinion; unhappy with their current artificial eye)
  • 4. Be able to self-complete the English language outcome measure tools (or can complete with assistance)

排除标准

  • 1. Ongoing clinical concerns with respect to their artificial eye use, such as poor eye socket healing, infections, extrusion, dehiscence
  • 2. Lacks capacity or willingness to provide consent to participate in the study
  • 3. Pregnant women or persons currently shielding (due to ongoing COVID-19 pandemic, to avoid unnecessary visits to the clinic)
  • 4. Is currently participating in another study evaluating their artificial eye
  • 5. Has been previously recruited for this study
  • 6. Has bilateral artificial eyes
  • 7. Is deemed to be not clinically appropriate to take part in the study (at clinician discretion)

研究者

发起方
eeds Teaching Hospitals NHS Trust

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