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临床试验/ACTRN12611000091909
ACTRN12611000091909招募中2 期

The effect of variable dosing Ranibizumab (Lucentis) and Sub-Tenon Triamcinolone (Kenacort-A 40) on visual acuity and number of intravitreal injections in patients with exudative age related macular degeneration.

Royal Adelaide Hospital0 个研究点目标入组 40 人开始时间: 2011年1月25日最近更新:
适应症

试验速览

阶段
2 期
状态
招募中
入组人数
40

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Randomised controlled trial
主要目的
Treatment
盲法
Blinded (masking used)

入排标准

年龄范围
50 Years 至 o limit(—)
性别
All

入选标准

  • Age 50 years or older.
  • Active primary or recurrent subfoveal choroidal neovascularization secondary to Age Related Macular Degeneration (ARMD).
  • Occular Coherence Tomography(OCT) central retinal thickness greater than 300 microns.
  • Best-corrected visual acuity (BCVA) of 20/40 to 20/400 (Snellen equivalent) in the study eye.
  • Adequate renal function (glomerular filtration calculated by Cockcroft/Gault formula or measure urine creatinine clearance > or = to 50 mL/minute)
  • In patients with bilateral presentation of exudative ARMD the eye of most recent onset will be enrolled.

排除标准

  • Previous subfoveal focal laser photocoagulation in the study eye.
  • Laser photocoagulation (juxtafoveal or extrafoveal) in the study eye within one month preceding day 0 (day of first injection).
  • Subfoveal fibrosis or atrophy in the study eye.
  • History of vitrectomy surgery in the study eye.
  • Aphakia or absence of the posterior capsule in the study eye.
  • History of idiopathic or autoimmune-associated uveitis (intraocular inflammation) in either eye.
  • Pregnancy. Sexually active pre-menopausal women will be required to have a serum Beta-Human chorionic gonadotropin (Beta-HCG) pregnancy test prior to each injection.
  • Uncontrolled glaucoma (defined as intraocular pressure >25 mmHg despite treatment with antiglaucoma medication).
  • Loss of vision due to other causes,
  • Systemic treatment with greater than or equal to 5 mg prednisolone (or equivalent) daily.
  • Intercurrent severe systemic disease.
  • Any condition affecting follow-up or documentation.
  • Active ocular, periocular or systemic infection.
  • Idiopathic thrombocytopaenic purpura.
  • Hypersensitivity to either Ranibizumab or Triamcinalone.
  • Known severe steroid responder.
  • Presence of a scleral buckle from previous retinal detachment surgery

研究者

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