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临床试验/ISRCTN42235351
ISRCTN42235351进行中(未招募)4 期

Correction of low level of astigmatism with soft contact lenses

CooperVision International Ltd0 个研究点目标入组 25 人开始时间: 2023年9月29日最近更新:
适应症

试验速览

阶段
4 期
状态
进行中(未招募)
发起方
入组人数
25

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

性别
All

入选标准

  • In order to be enrolled, each participant shall meet the following criteria:
  • 1. Aged 18 to 35 years
  • 2. Current contact lens wearer
  • 3. Spectacle refraction:
  • Distance: Sphere: -6.00D to + 2.00D
  • Astigmatism: -0.50D to -1.00D with at least -0.75D in one eye
  • 4. Best corrected visual acuity of at least 20/25 in each eye

排除标准

  • 1. Acute and subacute inflammation or infection of the anterior chamber of the eye
  • 2. Any eye disease, injury or abnormality that affects the cornea, conjunctiva or eyelids that would contraindicate contact lens wear
  • 3. Corneal hypoesthesia (reduced corneal sensitivity), if not aphakic
  • 4. Severe insufficiency of lacrimal secretion (dry eyes)
  • 5. Any systemic disease that may affect the eye or may be exaggerated by wearing contact lenses (e.g. acne and eczema)
  • 6. Allergic reactions of ocular surfaces or adnexa that may be induced or exaggerated by wearing contact lenses or use of contact lens solutions
  • 7. Any active corneal infection (bacterial, fungal, protozoal or viral)
  • 8. Newly prescribed (within the past 30 days) use of some systemic medications (such as antihistamines, decongestants, diuretics, muscle relaxants, tranquilizers, stimulants, anti-depressants, anti-psychotics, oral contraceptives) or new prescription eyedrops which is not rewetting/lubricating eyedrops for which contact lens wear could be contraindicated as determined by the investigator
  • 9. Monocular participants (only one eye with functional vision) or participants fit with only one contact lens
  • 10. Subjects with slit lamp findings greater than grade 1 (e.g. edema, infiltrates, corneal neovascularization, corneal staining, tarsal abnormalities, conjunctival, anterior segment inflammation) as per ISO 11980, any previous history or signs of a contact lens related corneal inflammatory event (past corneal ulcers), or any other ocular abnormality that may contraindicate contact lens wear at the enrolment visit
  • 11. History of corneal refractive surgery
  • 12. Enrolment of the family members of the investigator, family members of the investigator’s staff, or individuals living in the households of these individuals
  • 13. Current wearer of the control contact lenses MyDay® spherical or the test contact lenses MyDay Toric®

研究者

发起方
CooperVision International Ltd

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