NCT06250322已完成不适用
A Multicenter, Observational, Single Arm Study of the TECNIS Presbyopia-correcting Intraocular Lens
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 307
- 试验地点
- 37
- 主要终点
- Visual Symptoms
研究概览
简要总结
Ambispective post-market data collection on visual symptoms, patient satisfaction and surgeon experience with the TECNIS PC IOL.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Other
入排标准
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Patients who are bilaterally implanted with TECNIS PC IOL and are at least 45 days postoperative from their second eye surgery
- •Clear intraocular media
- •Signed informed consent and data protection documentation
- •Availability, willingness, ability, and sufficient cognitive awareness to comply with examination procedures
- •Ability to understand, read, and write English or the local language in which the informed consent and questionnaires are provided
排除标准
- •Subjects with ongoing adverse events that might impact outcomes during the study
- •Use of systemic or ocular medication that may affect vision
- •Acute or chronic disease or condition, ocular trauma or surgery that may confound results
- •Patients with amblyopia, strabismus, nystagmus
- •Concurrent participation in another clinical trial
结局指标
主要结局
Visual Symptoms
时间窗: 3month postoperative
Patient questionnaires
Surgeon Experience
时间窗: 3month postoperative
Questionnaire
Visual Acuity
时间窗: 3month postoperative
Visual Acuity will be collected with standard clinical charts.
次要结局
未报告次要终点
研究者
研究点 (37)
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