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临床试验/NCT03578926
NCT03578926已完成不适用

Performance of Toric Silicone Hydrogel Contact Lenses Following Two Weeks of Daily Wear

Coopervision, Inc.1 个研究点 分布在 1 个国家目标入组 45 人开始时间: 2018年6月18日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
45
试验地点
1
主要终点
Post Blink Movement

研究概览

简要总结

Prospective study to evaluate the clinical performance of fanfilcon A toric contact lens and senofilcon A toric contact lens after two weeks of wear.

详细描述

The aim of this prospective study is to evaluate the clinical performance of Avaira Vitality toric and ACUVUE OASYS® for ASTIGMATISM contact lenses after 2-weeks of wear in each pair.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Treatment
盲法
Double (Participant, Investigator)

盲法说明

Double masked (participant and investigator)

入排标准

年龄范围
18 Years 至 40 Years(Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Is between 18 and 40 years of age (inclusive)
  • •Has had a self-reported visual exam in the last two years
  • •Is an adapted soft contact lens wearer
  • •Has a contact lens spherical prescription between +6.00 to - 9.00 (inclusive)
  • •Have no less than -0.75D of astigmatism and no more than -2.25 D in both eyes.
  • •Can achieve best corrected spectacle distance visual acuity of 20/25 (0.10 logMAR) or better in each eye.
  • •Can achieve a distance visual acuity of 20/30 (0.18 logMAR) or better in each eye with the study contact lenses.
  • •Has clear corneas and no active ocular disease
  • •Has read, understood and signed the information consent letter.
  • •Patient contact lens refraction should fit within the available parameters of the study lenses.
  • •Is willing to comply with the wear schedule (at least 5 days per week, > 8 hours/day assuming there are no contraindications for doing so).
  • •Is willing to comply with the visit schedule

排除标准

  • •Has a CL prescription outside the range of the available parameters of the study lenses.
  • •Has a spectacle cylinder less than -0.75D or more than -2.50 D of cylinder in either eye.
  • •Has a history of not achieving comfortable CL wear (5 days per week; > 8 hours/day)
  • •Has contact lens best corrected distance vision worse than 20/25 (0.10 logMAR) in either eye.
  • •Presence of clinically significant (grade 2-4) anterior segment abnormalities
  • •Presence of ocular or systemic disease or need of medications which might interfere with contact lens wear.
  • •Slit lamp findings that would contraindicate contact lens wear such as:
  • •Pathological dry eye or associated findings
  • •Pterygium, pinguecula, or corneal scars within the visual axis
  • •Neovascularization > 0.75 mm in from of the limbus
  • •Giant papillary conjunctivitis (GCP) worse than grade 1
  • •Anterior uveitis or iritis (past or present)
  • •Seborrheic eczema, Seborrheic conjunctivitis
  • •History of corneal ulcers or fungal infections
  • •Poor personal hygiene
  • •Has a known history of corneal hypoesthesia (reduced corneal sensitivity)
  • •Has aphakia, keratoconus or a highly irregular cornea.
  • •Has Presbyopia or has dependence on spectacles for near work over the contact lenses.
  • •Has undergone corneal refractive surgery.
  • •Is participating in any other type of eye related clinical or research study.

研究组 & 干预措施

fanfilcon A toric lens

Experimental

Randomized participants will wear fanfilcon A toric contact lenses bilaterally for two weeks then switch to senofilcon A toric contact lenses for another two weeks.

干预措施: fanfilcon A toric lens (Device)

senofilcon A toric lens

Active Comparator

Randomized participants will wear senofilcon A toric contact lenses bilaterally for two weeks then switch to fanfilcon A toric contact lenses for another two weeks.

干预措施: senofilcon A toric lens (Device)

结局指标

主要结局

Post Blink Movement

时间窗: 2 weeks

Amount of lens movement after blink (0-5 Likert Scale, 0=Insufficient, 2=Optimal, 4=Excessive movement)

Lens Centration

时间窗: 2 weeks

Centration of lens on eye (Optimum, Decentration acceptable, Decentration unacceptable)

Corneal Coverage

时间窗: 2 weeks

Lens covering the cornea (Yes, No)

Corneal Coverage

时间窗: Baseline

Lens covering the cornea (Yes, No)

Lens Centration

时间窗: Baseline

Centration of lens on eye (Optimum, Decentration acceptable, Decentration unacceptable)

Post Blink Movement

时间窗: Baseline

Amount of lens movement after blink (0-5 Likert Scale, 0=Insufficient, 2=Optimal, 4=Excessive movement)

次要结局

  • Wearing Time(2 weeks)
  • Comfortable Wearing Time(2 weeks)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (1)

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