NCT02146599已完成不适用
Patient Perception of Visual Quality and Function
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
- 是
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
研究点 (1)
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