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临床试验/EUCTR2010-023037-35-GB
EUCTR2010-023037-35-GB进行中(未招募)不适用

Short-term intraocular pressure trends in high risk patients following intravitreal Ranibizumab (Lucentis) injections for Wet Age Related Macular Degeneration - Is there a role for systemic Acetazolamide (Diamox) in those with glaucoma? - LIEPS - Lucentis Injection Eye Pressure Study

York Teaching Hospital NHS Foundation Trust0 个研究点目标入组 24 人开始时间: 2010年12月6日最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
24

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • The sample group will include glaucoma and glaucoma suspect patients undergoing intravitreal injections for neovascular (wet) AMD at York Hospital.
  • 1.Patients with neovascular (wet) AMD requiring Lucentis injections
  • 2.Glaucoma or Glaucoma suspect
  • 3.Written informed consent
  • 4. Baseline pre injection Intraocular Pressure of less than 30 mmHg
  • Are the trial subjects under 18? no
  • Number of subjects for this age range: 0
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 0
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 24

排除标准

  • 1.Baseline pre-injection IOP of 30 mmHg or higher
  • 2.Unable to give written informed consent
  • 3.Known allergy to sulphur containing drugs or acetazolamide
  • 4. 18 years or younger
  • 5. Marked kidney or liver disease/dysfunction
  • 6. Supra-renal gland failure
  • 7. Hypercholrcmic adcidosis
  • 8. Hepatic cirrhosis
  • 9. Pregnancy and pre-menopausal women
  • 10. Concomitant use of other oral carbonic anhydrase inhibitors apart from acetazolamide

研究者

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