ACTRN12622000709741尚未招募未知
A prospective, non-randomized, non-dispensing clinical trial to assess the objective and subjective visual performance of ophthalmic lens prototypes (PESTA Study) in adults.
适应症
试验速览
- 阶段
- 未知
- 状态
- 尚未招募
- 入组人数
- 10
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Non-randomised trial
- 主要目的
- Treatment
- 盲法
- Open (masking not used)
入排标准
- 年龄范围
- 18 Years 至 o limit(—)
- 性别
- All
入选标准
- •Able to read and comprehend English and give informed consent as demonstrated by signing a record of informed consent. Be 18years and above.
- •- Willing to comply with the wearing of the study lenses and the clinical trial visit schedule as directed by the Investigator.
- •- Have ocular health findings considered to be normal”
- •- Spherical prescription range of +6.00D to -6.00DS inclusive and astigmatism <-2.00DC.Reading add power of <+3.00D
- •- Vision of 6/7.5 (20/25) or better in each eye with or without correction.
- •- Spectacle and/or contact lens wearers or participants not requiring any optical correction.
排除标准
- •- Have strabismus and/or amblyopia.
- •- Use of or a need for any systemic medication or topical medications which may alter normal ocular findings / are known to affect a participant’s ocular health / physiology or contact lens performance either in an adverse or beneficial manner at enrolment and/or during the clinical trial.
- •- Any systemic disease that adversely affects ocular health e.g. diabetes, Graves’ disease, and autoimmune diseases such as ankylosing spondylitis, multiple sclerosis, Sjogren’s syndrome and systemic lupus erythematosus. Conditions such as systemic hypertension and arthritis do not automatically exclude prospective participants.
- •- Eye surgery within 12 weeks immediately prior to enrolment for this trial.
- •- Previous corneal refractive surgery.
- •- Known allergy or intolerance to ingredients in any of the clinical trial products.
- •- Pregnancy*.
- •The Investigator may, at his/her discretion, exclude anyone who they believe may not be able to fulfil the clinical trial requirements or it is believed to be in the participant’s best interests.*Formal testing of pregnancy is not required. A participant’s verbal report is sufficient.
研究者
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