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临床试验/DRKS00030330
DRKS00030330已完成不适用

Impact of corneal collagen cross-linking on vision-related quality of life in patients with progressive keratoconus - QoL in progressive Keratoconus

Augenklinik des Universitätsklinikums Hamburg-Eppendorf (UKE)0 个研究点目标入组 41 人开始时间: 2022年10月4日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
41

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
12 Years 至 one(—)
性别
All

入选标准

  • keratoconus (See reference [1]):
  • -KISA-index >100 mit I-S >1.4 and/or Kmax>47
  • -progressive keratoconus:
  • (based on the „Global consensus on keratoconus and extatic diseases[2]): Changes in at least two of the following categories:
  • 1. progressive steepening of the anterior corneal surface (topography)
  • 2. progressive steepening of the posterior corneal surface (tomography)
  • 3. progressive thinning of the corneal thickness
  • -> no specific cut-offs due to the recommendation of the „global consensus because different diagnostic devices were used for diagnosing keratoconus (Oculus Pentacam; Ziemer Galilei).
  • -> in case of missing corneal diagnostic data to determine a potential progression of the disease, the following alternative criteria are used [3]:
  • -decrease of the best corrected visual acuity >= 2 lines (decimal)
  • -increase of the refractive astigmatism and/ or the spherical equivalent >= 1 diopter
  • [1]: Rabinowitz YS, Rasheed K. KISA% index: a quantitative videokeratography al-gorithm embodying minimal topographic criteria for diagnosing keratoconus. J Cat-aract Refract Surg 1999; 25(10): 1327-35.
  • [2]: Gomes JA, Rapuano CJ, Belin MW, et al. Global Consensus on Keratoconus Diagnosis. Cornea 2015; 34(12): e38-9.
  • [3]: Hashemi H, Seyedian MA, Miraftab M, et al. Corneal collagen cross-linking with riboflavin and ultraviolet a irradiation for keratoconus: long-term results. Ophthalmo-logy 2013; 120(8): 1515-20.

排除标准

  • -previous ocular surgery
  • -previous ocular trauma
  • -stopp of contact lens wearing before the measurements <3 days (soft contact lenses) or < 5 days (hard contact lenses)
  • -unwillingness to participate in the study/ the necessary follow-up examinations.
  • -no written consent form (participation on the study)

研究者

发起方
Augenklinik des Universitätsklinikums Hamburg-Eppendorf (UKE)

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