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临床试验/NCT02173535
NCT02173535已完成不适用

Quantitative Study of New Limbal Ring Prototypes

Johnson & Johnson Vision Care, Inc.1 个研究点 分布在 1 个国家目标入组 257 人开始时间: 2014年5月1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
257
试验地点
1
主要终点
Number of Subject in Agreement (Bigger Eyes)

研究概览

简要总结

The study is designed to test five new soft contact lens color pattern variants to determine whether the test lens makes the wearers eyes look bigger, more defined or enhances their overall appearance.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Other
盲法
None

入排标准

年龄范围
18 Years 至 39 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • The subject must be at least 18 years of age and no more than 39 years of age (inclusive)
  • Subjects must be Asian female
  • Subjects must be able to read Chinese
  • Subjects' monthly household income must be above HKD$ 10,000
  • Subjects must be habitual soft contact lens wearer or habitual limbal lens wearer or have a history of previous habitual lens wear.
  • Subjects' current/previous habitual lens must be in the disposable soft lens modality (ranging from daily to monthly)
  • Subjects must have dark colored iris (black, brown, or brown hazel)
  • Subjects must be "concept acceptors". Concept acceptors are subjects that are willing to try new circle contact lenses.
  • Subjects must be classified as either 'Classic' or 'Vogue' on a Pattern Evaluation Screening Questionnaire.
  • Subjects must have acceptable near vision (without vision correction) and be able to see the test article lenses in the mirror 30 cm or closer.
  • Subjects must have best corrected visual acuity of 20/40 (Snellen or equivalent) or better in each eye.
  • Subjects must possess a functional/usable pair of spectacles and bring them to the visit (only if applicable-to the investigators discretion)
  • Subjects must read, understand, and sign the Statement of Informed Consent
  • Subjects must appear able and willing to adhere to the instructions set forth in this clinical protocol

排除标准

  • Subjects, or subjects' family member within the same household, that work for the following entities/companies: Government, advertising, marketing research or consultancy, media or public relations, companies that make, distribute or sell eyewear or contact lenses, eyecare practice (optometrist, ophthalmologist, optician) or the research center conducting the study
  • Habitual wearers of rigid gas permeable lenses within the last 3 months
  • Habitual soft conventional contact lens wearers (conventional lenses defined as replacement modality of greater than 1 month)
  • Any color deficiencies, by self report
  • Currently pregnant or breast-feeding a baby
  • Any ocular or systemic allergies or diseases which may interfere with contact lens wear
  • Any systemic disease, autoimmune disease, or use of medication which may interfere with contact lens wear, at the investigator's discretion
  • Any infectious diseases (e.g. hepatitis, tuberculosis) or a contagious immunosuppressive disease (e.g. HIV), by self report
  • Any grade 3 or greater Biomicroscopy findings (this includes, corneal edema, corneal staining, corneal vascularization, conjunctival injection, tarsal abnormalities, bulbar injection) on the FDA classification scale
  • Any active ocular abnormalities/conditions that may interfere with contact lens wear (this includes, but not limited to, chalazia, recurrent styes, pterygium, infection, etc.)
  • Any corneal distortion or moderate or above corneal distortion by self report
  • History of any corneal refractive surgery
  • Habitual contact lens is multifocal, monovision or worn as extended wear

研究组 & 干预措施

etafilcon test contact lens Variant JG

Experimental

干预措施: etafilcon test contact lens Variant AP (Device)

etafilcon test contact lens Variant JG

Experimental

干预措施: etafilcon test contact lens Variant JG (Device)

etafilcon test contact lens Variant JG

Experimental

干预措施: etafilcon test contact lens Variant CS (Device)

etafilcon test contact lens Variant JG

Experimental

干预措施: etafilcon test contact lens Variant VC (Device)

etafilcon test contact lens Variant JG

Experimental

干预措施: etafilcon test contact lens Variant LA (Device)

etafilcon test contact lens Variant CS

Experimental

干预措施: etafilcon test contact lens Variant AP (Device)

etafilcon test contact lens Variant CS

Experimental

干预措施: etafilcon test contact lens Variant JG (Device)

etafilcon test contact lens Variant CS

Experimental

干预措施: etafilcon test contact lens Variant CS (Device)

etafilcon test contact lens Variant CS

Experimental

干预措施: etafilcon test contact lens Variant VC (Device)

etafilcon test contact lens Variant CS

Experimental

干预措施: etafilcon test contact lens Variant LA (Device)

etafilcon test contact lens Variant VC

Experimental

干预措施: etafilcon test contact lens Variant AP (Device)

etafilcon test contact lens Variant LA

Experimental

干预措施: etafilcon test contact lens Variant LA (Device)

etafilcon test contact lens Variant VC

Experimental

干预措施: etafilcon test contact lens Variant JG (Device)

etafilcon test contact lens Variant VC

Experimental

干预措施: etafilcon test contact lens Variant CS (Device)

etafilcon test contact lens Variant VC

Experimental

干预措施: etafilcon test contact lens Variant VC (Device)

etafilcon test contact lens Variant VC

Experimental

干预措施: etafilcon test contact lens Variant LA (Device)

etafilcon test contact lens Variant LA

Experimental

干预措施: etafilcon test contact lens Variant AP (Device)

etafilcon test contact lens Variant LA

Experimental

干预措施: etafilcon test contact lens Variant JG (Device)

etafilcon test contact lens Variant LA

Experimental

干预措施: etafilcon test contact lens Variant CS (Device)

etafilcon test contact lens Variant LA

Experimental

干预措施: etafilcon test contact lens Variant VC (Device)

etafilcon test contact lens Variant AP

Experimental

干预措施: etafilcon test contact lens Variant AP (Device)

etafilcon test contact lens Variant AP

Experimental

干预措施: etafilcon test contact lens Variant JG (Device)

etafilcon test contact lens Variant AP

Experimental

干预措施: etafilcon test contact lens Variant CS (Device)

etafilcon test contact lens Variant AP

Experimental

干预措施: etafilcon test contact lens Variant VC (Device)

etafilcon test contact lens Variant AP

Experimental

干预措施: etafilcon test contact lens Variant LA (Device)

结局指标

主要结局

Number of Subject in Agreement (Bigger Eyes)

时间窗: 15-20 Minutes Post Lens Insertion

Subjects' responses to the question "Make my eye look bigger" were categorized into a binary variable. If a subject responded "Agrees Somewhat" or "Agrees Strongly" then response=1. If a subject responds "Neither Agrees nor Disagrees", "Disagrees Somewhat" "Disagrees Strongly" then response=0. The number of subjects with response=1 was reported for each lens.

Number of Subject in Agreement (Defines Eyes)

时间窗: 15-20 Minutes Post Lens Insertion

Subjects' responses to the question "Define my eye" were categorized into a binary variable. If a subject responded "Agrees Somewhat" or "Agrees Strongly" then response=1. If a subject responds "Neither Agrees nor Disagrees", "Disagrees Somewhat" "Disagrees Strongly" then response=0. The number of subjects with response=1 was reported for each lens.

Number of Subject in Agreement (Enhance Eyes)

时间窗: 15-20 Minutes Post Lens Insertion

Subjects' responses to the question "Enhance my overall appearance" were categorized into a binary variable. If a subject responded "Agrees Somewhat" or "Agrees Strongly" then response=1. If a subject responds "Neither Agrees nor Disagrees", "Disagrees Somewhat" "Disagrees Strongly" then response=0. The number of subjects with response=1 was reported for each lens.

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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Quantitative Study of New Limbal Ring Prototypes | 临床试验