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临床试验/ISRCTN58543190
ISRCTN58543190已完成未知

Recombinant tissue Plasminogen Activator administration by retinal branch vein route for Central Retinal Vein Occlusion: a randomised conventional therapy controlled trial

Oogziekenhuis Rotterdam (OZR) (The Netherlands)0 个研究点目标入组 48 人开始时间: 2006年9月26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
48

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. Informed consent
  • 2. Over 18 years of age
  • 3. Adequate birth control (if not post-menopausal or sterilised) during a two week pre- and six week post-operative period if assigned to vitreoretinal surgery
  • 4. Subjective decrease in visual acuity starting within four weeks prior to study start, due to CRVO, clinically evident by fundoscopy
  • 5. Non-perfused or perfused CRVO with a visual acuity of less than 20/200
  • Note : Pseudophakic patients are allowed to participate in this study.

排除标准

  • 1. Inability to visualize fundus due to corneal or important lenticular opacities
  • 2. Inability to obtain photographs of CRVO due to allergy to fluorescein or lack of veinous access
  • 3. As visual acuity prognosis is better and risk for neovascularisation is reduced in perfused CRVO, patients with a visual acuity of more than 20/200 will not be included
  • 4. Presence of iris neovascularisation (more than grade one) or anterior chamber angle (more than grade one) at the moment of presentation
  • 5. Other retinal or ophthalmic disorders that could influence the macular area
  • 6. Disorders that could be complicated by iris or retinal neovascularisation
  • 7. Disorders that could be complicated by any form of secondary glaucoma
  • 8. Prescription of acetazolamide or high dose systemic steroid (more than 10 mg prednisone daily) or other anti-inflammatory medication (eg. Methotrexate (MTX), Imuran, Endoxan, Humira, Kineret, Infliximab, Thalidomide) except Non Steriodal Anti-Inflammatory Drugs (NSAIDs)
  • 9. Participation in another clinical ophthalmic trial
  • 10. Any surgery of the orbit, ocular adnexae or eye scheduled during the period the study (except for cataract surgery, developed after inclusion to a degree as outlined by the protocol)
  • 11. Monophthalmia or other known ophthalmic disorder in the fellow eye that could be complicated by blindness
  • 12. Previous retinal surgery
  • 13. High myopia (-8 D spherical equivalent or more)
  • 14. Macula affecting drugs

研究者

发起方
Oogziekenhuis Rotterdam (OZR) (The Netherlands)

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