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Surface Refractive Index Shift of Kalifilcon A Compared With Dailies Total1 and Precision1 Lenses

2026年8月3日 更新者:Bausch & Lomb Incorporated

Evaluation of Surface Refractive Index Shift and Lens Absorption / Adsorption of Tear Components of Commercially Available Kalifilcon A Lenses Compared to Dailies Total1 and Precision1

This was a single-site, bilateral, repeated-measures insertion study in habitual soft contact lens wearers. Ten participants were enrolled. All participants attended a Screening/Dispensing Visit at which informed consent was obtained and eligibility was assessed. Eligible participants then wore each of three commercially available daily disposable soft contact lens types - kalifilcon A (Bausch + Lomb), Dailies Total1 (delefilcon A, Alcon) and Precision1 (verofilcon A, Alcon), all -3.00 D - bilaterally for wear times of 0.5, 1, 3, 5 and 10 minutes over a total of 6 study visits. A new lens pair was inserted for each wear time, with a 3-5 minute washout period between lens pairs. Immediately following removal, the right-eye lens was measured for surface refractive index on a Metricon M-2010 Prism Coupler.

研究概览

详细说明

Rationale: earlier work (ROC2-20-012) showed a change in surface refractive index for Dailies Total1 (delefilcon A) and Precision1 (verofilcon A) lenses after 5 minutes of wear, attributed to a change in surface water content. ROC2-21-007 was designed to determine whether that change occurs in less than 5 minutes. Three study lenses (one test, two controls) were each worn bilaterally. Wear times of 0.5, 1 and 3 minutes were completed at one visit and 5 and 10 minutes at another visit for each lens type, giving 6 visits of approximately 30 minutes each, each on a separate day; the clinical investigation took approximately 2 weeks. Lens type order followed the study randomization schedule prepared before enrolment by an unmasked statistician not otherwise involved in the study; unmasked study personnel dispensed and collected study materials so that the participant and Investigator remained masked. Endpoint: surface refractive index of the worn right-eye lens, measured on a Metricon M-2010 Prism Coupler, compared with unworn (baseline) values for the same lens types. Continuous data were summarized with n, mean, standard deviation, median, minimum and maximum, and paired t-tests were used to compare unworn with worn values, with p < 0.05 considered statistically significant.

研究类型

介入性

注册 (实际的)

10

阶段

  • 不适用

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

    • New York
      • Rochester、New York、美国、14609
        • Bausch & Lomb Incorporated

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

18年 及以上 (成人、年长者)

接受健康志愿者

是的

描述

Inclusion Criteria:

  1. Be 18 years or older and have full legal capacity to volunteer.
  2. Have physiologically normal anterior segments not exhibiting clinically significant biomicroscopy findings.
  3. Have no active ocular disease or allergic conjunctivitis.
  4. Not be using any topical ocular medications.
  5. Be willing and able to follow instructions.
  6. Have signed a statement of informed consent.

Exclusion Criteria:

  1. Participating in a conflicting study in the opinion of the Investigator.
  2. Considered by the Investigator to not be a suitable candidate for participation.

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:基础科学
  • 分配:不适用
  • 介入模型:单组作业
  • 屏蔽:无(打开标签)

武器和干预

参与者组/臂
干预/治疗
其他:All Participants: kalifilcon A, Then Dailies Total1, Then Precision1
Each participant wore all three study lens types bilaterally, one lens type per pair of visits, in the order specified by the study randomization schedule (kalifilcon A, then Dailies Total1, then Precision1). For each lens type a new lens pair was inserted for each wear time of 0.5, 1, 3, 5 and 10 minutes, with a 3-5 minute washout period between lens pairs. Wear times of 0.5, 1 and 3 minutes were completed at one visit and 5 and 10 minutes at another visit, for a total of 6 visits. Immediately after removal the right-eye lens was measured for surface refractive index on a Metricon M-2010 Prism Coupler.
Commercially available Infuse (kalifilcon A) daily disposable spherical soft contact lens, -3.00 D, worn bilaterally for 0.5, 1, 3, 5 and 10 minutes.
其他名称:
  • 注入
Commercially available Dailies Total1 (delefilcon A) daily disposable spherical soft contact lens (Alcon), -3.00 D, worn bilaterally for 0.5, 1, 3, 5 and 10 minutes.
Commercially available Precision1 (verofilcon A) daily disposable spherical soft contact lens (Alcon), -3.00 D, worn bilaterally for 0.5, 1, 3, 5 and 10 minutes.

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Surface Refractive Index of Worn Lenses
大体时间:Unworn lens (baseline) and immediately after 0.5, 1, 3, 5, and 10 minutes of lens wear
Immediately following lens removal, the right-eye worn lens for each participant was measured for surface refractive index on a Metricon M-2010 Prism Coupler. A new lens pair was worn for each wear time. Surface refractive index is a dimensionless ratio and has no units.
Unworn lens (baseline) and immediately after 0.5, 1, 3, 5, and 10 minutes of lens wear

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

调查人员

  • 首席研究员:Jeffery Schafer, OD, MS、Bausch & Lomb Incorporated

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (实际的)

2021年4月7日

初级完成 (实际的)

2021年4月15日

研究完成 (实际的)

2021年4月15日

研究注册日期

首次提交

2021年4月7日

首先提交符合 QC 标准的

2021年4月8日

首次发布 (实际的)

2021年4月12日

研究记录更新

最后更新发布 (实际的)

2026年8月5日

上次提交的符合 QC 标准的更新

2026年8月3日

最后验证

2026年8月1日

更多信息

与本研究相关的术语

关键字

其他研究编号

  • ROC2-21-007

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

IPD 计划说明

Individual participant data will not be shared. This was an internal Bausch + Lomb device performance study; source data are retained in the Trial Master File.

药物和器械信息、研究文件

研究美国 FDA 监管的药品

研究美国 FDA 监管的设备产品

是的

在美国制造并从美国出口的产品

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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