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临床试验/NCT06364761
NCT06364761尚未招募不适用

Assesment of Intermediate and Near Vision After Bag in the Lens Cataract Surgery

Universitair Ziekenhuis Brussel0 个研究点目标入组 38 人开始时间: 2024年4月最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
入组人数
38
主要终点
Intermediate vision

研究概览

简要总结

The goal of this observational study is to learn about the intermediate and near vision in patiënts who underwent cataract surgery with a specific technique, called "bag in the lens".

The main question it aims to answer is whether patiens who underwent this type of cataract surgery have better intermediate vision without spectacle correction than patients who underwent the classic lens in the bag cataract surgery.

Participants will:

  • Have to read with and without spectacle correction at different distances (4 meters, 66 centimeters, 40 centimeters)
  • Have to fill in 2 questionnaires about visual functioning and spectacle independance

Researchers will compare these values to the same values from the standard population who underwent the classic lens in the bag cataract surgery with a monofocal intraocular lens .

研究设计

研究类型
Observational
观察模型
Case Only
时间视角
Cross Sectional

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients of at least 18 years old
  • Must have underwent bilateral bag in the lens cataract surgery in the University hospital Brussels at least 3 months before inclusion
  • Must not meet any exclusion criteria

排除标准

  • Prior refractive surgery (other than bag in the lens)
  • Corneal opacities
  • Moderate non proliferative diabetic retinopathy or worse
  • Optic neuropathy
  • History of uveitis
  • Amblyopia
  • Residual post-operative astigmatism higher than 1.5 Diopters (D)
  • Best corrected visual acuity < 1.0
  • Patients unable to cooperate or sign the informed consent

结局指标

主要结局

Intermediate vision

时间窗: During the only hospital visit required in the study, between april and december 2024

uncorrected and distance corrected intermediate vision at 66cm in LogMAR

次要结局

  • Near vision(During the only hospital visit required in the study, between april and december 2024)

研究者

申办方类型
Other
责任方
Sponsor

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