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临床试验/ISRCTN66216819
ISRCTN66216819已完成3 期

An exploratory phase III prospective open-label clinical study on monthly Optical Coherence Tomography (OCT) monitoring of the effects of Ozurdex for macular oedema related to retinal vascular diseases (OCTOME Study)

King's College NHS Foundation Trust (UK)0 个研究点目标入组 30 人开始时间: 2011年6月29日最近更新:

试验速览

阶段
3 期
状态
已完成
发起方
入组人数
30

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. Aged 18 or above
  • 2. Ability to provide informed consent
  • 3. Diagnosis of macular oedema secondary to diabetic maculopathy, branch and central retinal vein occlusion or pseudophakic cystoid macular oedema or post-inflammatory macular oedema
  • 4. Central macular thickness on OCT should be above 250µm
  • 5. Best corrected visual acuity in the study eye between 37 and 68 letters

排除标准

  • 1. Any other eye disease which could mask macular oedema
  • 2. Known uncontrolled systemic disease or current immunosuppressive disease
  • 3. Initiation of medical therapy for diabetes or a change from oral hypoglycaemic agents to insulin therapy within 4 months prior to the screening visit
  • 4. Renal failure requiring haemodialysis or peritoneal dialysis within 6 months prior to screening visit
  • 5. Any ocular condition in the study eye that in the opinion of the investigator would prevent a 15-letter improvement in visual acuity (e.g., severe macular ischemia, extensive macular laser scarring or atrophy)
  • 6. Presence of an epiretinal membrane or vitreo-retinal interface changes in the study eye which, in the opinion of the investigator, is the primary cause of macular oedema, or is severe enough to prevent improvement in visual acuity despite reduction in macular oedema
  • 7. Active or suspected ocular or periocular infection including most viral diseases of the cornea and conjunctiva, including active epithelial herpes simplex keratitis (dendritic keratitis), vaccinia, varicella, mycobacterial infections, and fungal diseases
  • 8. Advanced glaucoma which cannot be adequately controlled by medicinal products alone
  • 9. History of IOP elevation in response to steroid treatment in either eye that resulted in any of the following:
  • 9.1. >10 mm Hg increase in IOP from baseline with an absolute IOP > 25 mm Hg
  • 9.2. Required therapy with 3 or more anti-glaucoma medications
  • 10. Pregnancy if child bearing age (confirmed by pregnancy test) and to avoid pregnancy during the 36 weeks of the study. Pregnancy test will not be done in post-menopausal women (defined as 12 months post LMP)
  • 11. Breast feeding women will be excluded
  • 12. Hypersensitivity to the active substance or to any of the excipients
  • 13. Inability to provide informed consent

研究者

发起方
King's College NHS Foundation Trust (UK)

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