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临床试验/ISRCTN40512708
ISRCTN40512708已完成不适用

Corneal Glue Study: effect of corneal adhesive on preventing fluid ingress after cataract surgery ? a randomised control trial

Whipps Cross University Hospital (UK)0 个研究点目标入组 20 人开始时间: 2013年2月25日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
20

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

性别
All

入选标准

  • 1. Fit and well
  • 2. Uncomplicated cataract surgery
  • 3. Male and female patients over 45 years of age

排除标准

  • 1. Any patient regarded as having clinically significant blepharitis (contraindication to use of biodendrimer glue)
  • 2. Any patient requiring a general, subtenons or peribulbar anaesthetic
  • 3. Any patient requiring intraoperative trypan blue for capsular visualization
  • 4. Any patient who has an intraoperative complication including capsular rupture, zonular dehiscence, suprachoriodal haemorrhage and vitreous loss
  • 5. Any patient who is found to have an actively leaking wound at the end of surgery
  • 6. Patients aged 45 or younger
  • 7. Patients having undergone previous surgery (i.e., vitrectomy, glaucoma filtration surgery)
  • 6. Patients with pre-existing corneal disease (i.e., keratoconus, Fuch?s endothelial dystrophy)
  • 8. Patients who lack the capacity to consent for cataract surgery (i.e., those who would need a consent form 4 or consultant consent signed for them in their best interests)

研究者

发起方
Whipps Cross University Hospital (UK)

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