跳至主要内容
临床试验/NCT02146599
NCT02146599已完成不适用

Patient Perception of Visual Quality and Function

Abbott Medical Optics1 个研究点 分布在 1 个国家目标入组 301 人开始时间: 2014年5月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
301
试验地点
1
主要终点
Use of Corrective Visual Aids (i.e., Spectacles, Contact Lenses) Post Intraocular Lens (IOL) Surgery

研究概览

简要总结

The purpose of this study is to evaluate the visual quality and function of pseudophakic patients.

研究设计

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

入排标准

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

入选标准

  • Minimum 22 years of age
  • Pseudophakic patients who have been bilaterally implanted with the same type of intraocular lenses in both eyes
  • Ability to understand, read and write English to give consent and complete the study questionnaires
  • Availability, willingness, and sufficient cognitive awareness to comply with examination procedures and study visits
  • Signed informed consent and Health Insurance Portability and Accountability Act (HIPAA) authorization
  • Other protocol-defined inclusion criteria might apply

排除标准

  • Any ocular pathology of clinical significance, as determined by the investigator, that may affect visual outcomes or influence subjective ocular/visual symptoms
  • Patient is pregnant or is lactating
  • Concurrent participation or participation within 30 days prior in any other clinical trial
  • Other protocol-defined exclusion criteria might apply

结局指标

主要结局

Use of Corrective Visual Aids (i.e., Spectacles, Contact Lenses) Post Intraocular Lens (IOL) Surgery

时间窗: Baseline and 1 week

Patients will be assessed at a baseline visit and a visit 1 week later to determine their use of corrective visual aids (i.e., spectacles, contact lenses) post Intraocular Lens (IOL) surgery.

次要结局

未报告次要终点

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (1)

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