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
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