ISRCTN31552904已完成未知
Determination of corneal biomechanical properties in-vivo using a contact device: a single-arm, observational study
niversity of Liverpool (UK)0 个研究点目标入组 70 人开始时间: 2014年7月23日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 70
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Observational
入排标准
- 性别
- All
入选标准
- •1. At least 18 years of age
- •2. Normal findings in the medical history unless the investigator considers an abnormality to be clinically irrelevant
- •3. Normal ophthalmic findings, other than high IOP
- •4. Astigmatism <2D
- •5. Potential to complete the study and comply with appropriate instructions
- •6. Signature on the informed consent form
排除标准
- •1. Corneal pathology or previous intra- or extra-ocular surgery, including refractive surgery (e.g., radial keratotomy, photorefractive keratotomy, LASIK, intracorneal ring), retinal surgery (e.g., buckle, photocoagulation), or implantation of a primary or secondary intraocular lens
- •2. Contact lens wearing within 3 days (rigid contact lenses) or 1 day (soft contact lenses) prior to study day
- •3. Inability to fully understand the ?informed consent?
- •4. Participants who are diabetic
研究者
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