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临床试验/NCT00841386
NCT00841386Unknown2 期

Treatment of Keratoconus Using Collagen Cross-Linking By Means of Topical Riboflavin and UV Light.

University at Buffalo2 个研究点 分布在 1 个国家目标入组 150 人开始时间: 2008年9月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
入组人数
150
试验地点
2
主要终点
Best corrected visual acuity

研究概览

简要总结

The purpose of this study is to determine the effectiveness of collagen cross-linking in the cornea in halting the progression and possibly partially reversing the effects of keratoconus. Keratoconus is a progressive weakening in the cornea that causes irregular astigmatism and thinning of the cornea. The overall effect is reduction of vision, and in more advanced cases, scarring of the cornea that may lead to the need for corneal transplantation. Cross-linking has been shown increase the rigidity of the cornea. The patients would be treated once and then followed over 24 months. .

详细描述

The goal is for two groups of approximately 66 patients to be included in the study. One eye from the first group will undergo treatment, while the second group of age matched individuals will serve as a control. It will be a prospective, randomized, blinded study. Each patient will be randomized at the beginning of enrollment in the study and will receive a randomization number. The following parameters will be followed: 1. Best corrected spectacle acuity (BCSA) 2. The steepest keratometry measurement (KMax) as measured by computerized corneal topography 3. Apical corneal thickness 4. Corneal mechanical resistance. These measurements will be repeated at 1 month, 3 months, 6 months, 12, 18, and 24 months following treatment.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Triple (Participant, Care Provider, Outcomes Assessor)

入排标准

年龄范围
16 Years 至 35 Years(Child, Adult)
性别
All
接受健康志愿者

入选标准

  • no prior history of ocular surgery
  • treatment eye must have a maximum corneal power of between 47 D and 60 diopters
  • corneal thickness must be greater than 400 µ
  • absence of corneal scarring
  • patients must meet the diagnostic criteria for keratoconus, which include one or more of the following features:
  • high myopia
  • corneal ectasia as viewed by slit-lamp exam or measured by pachometry
  • Vogt's striae
  • topographic findings of superior flattening and inferior steepening of the cornea
  • presence of Fleischer ring

排除标准

  • history of prior ocular surgery (history of contact lens use is not an exclusion criterion)
  • average corneal power > 60 D
  • presence of corneal scarring
  • corneal thickness 400 µ or less
  • history of herpes simplex virus keratitis
  • history of uveitis
  • pre-existing glaucoma

研究组 & 干预措施

Cross-linking treatment

Experimental

Topical anesthesia (lidocaine jelly 2%) will be used. The central 9 mm of corneal epithelium will be removed cautiously with an Amoils brush. Riboflavin 0.1% solution will be applied (10 mg riboflavin-5-phosphate in 10 ml dextran T-500 20% solution, supplied in a sterile, single dose container) to the cornea every 2-3 minutes for 15 minutes and then every 5 minutes thereafter. The UV source will be from the CBM VEGA X-linker (CSO, Florence, Italy). A wavelength of 370 nm will be used to direct 5.4 J/cm2 to the area of cornea debrided for 30 minutes. The distance from the UV source to the cornea will be 1.5 to 5.4 cm.

干预措施: Riboflavin-5-phosphate (Drug)

Sham treatment group

Sham Comparator

Topical anesthesia (lidocaine jelly 2%) will be used. Differing from the treatment group, no epithelium will be debrided, but instead, this step will be skipped and a 2% methylcellulose solution combined with 1% fluorescein dye will be applied to the cornea every 5 minutes for 30 minutes. The patient will be placed under the UV device, but instead of the UV light, the LED aiming beam will be applied for 30 minutes.

干预措施: Sham cross-linking (Drug)

结局指标

主要结局

Best corrected visual acuity

时间窗: 24 months

Spherical equivalent power of the cornea (Best spectacle refraction)

时间窗: 24 months

KMax: the maximum corneal curvature

时间窗: 24 months

Average corneal power of the cornea in the central 4 mm.

时间窗: 24 months

次要结局

  • Corneal resistance factor.(24 months)
  • Maximal posterior surface elevation of the cornea.(24 months)
  • Apical corneal thickness.(24 months)
  • Endothelial count.(24 months)

研究者

申办方类型
Other

研究点 (2)

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