KCT0002549招募中未知
A prospective, single-center, open-Label, investigator initiated trial to compare the efficacy and safety of non-contact tonometer(HNT-1/P) and goldmann applanation tonometer for intraocular pressure measurements
试验速览
- 阶段
- 未知
- 状态
- 招募中
- 入组人数
- 84
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional Study
入排标准
- 年龄范围
- 19(Year) 至 79(Year)（—）
- 性别
- All
入选标准
- •[i.120 eyes except advanced corneal astigmatism]
- •1. 19 =age= 80
- •2. 7 =IOP< 60 mmHg
- •3. 500 =CCT< 600 µm
- •4. subject with functional eyes
- •5. A person who voluntarily agree to participate and agreed in writing to consent form.
- •6. Those who can understand and follow the instructions and participate in the entire period of the clinical trial.
- •[ ii. 30eyes advanced corneal astigmatism]
- •1. 19 =age= 80
- •2. 7 =IOP< 60 mmHg
- •3. 500 =CCT< 600 µm
- •4. subject with functional eyes
- •5. A person who voluntarily agree to participate and agreed in writing to consent form.
- •6. Those who can understand and follow the instructions and participate in the entire period of the clinical trial.
- •7. Corneal astigmatism exceeding 3 Diopter
排除标准
- •[i.120 eyes except advanced corneal astigmatism]
- •1. those with one eye having eccentric fixation
- •2. At least one of the following:
- •-advanced corneal astigmatism
- •-those with corneal scarring or who have had corneal surgery including corneal laser surgery
- •-microphthalmos
- •-buphthalmos
- •(except ; In case there is no present symptom at screening time, despite history of dry eye.)
- •-lid squeezers, blepharospasm
- •-nystagmus
- •-keratoconus
- •-any other corneal or conjunctival pathology of infection
- •3. Wearing contact lenses Within 2 weeks of screening time
- •4. Known hypersensitivity to local anesthetic (ex; proparacaine hydrochloride) and Fluorescent pigment (ex; fluorescein)
- •5. Person who participates in other interventional clinical trials within a period of one month
- •6. Pregnant, breast-feeding, possibly pregnant women
- •7. Ineligible for participating in this study according to the investigator or sub-investigator.
- •[ ii. 30eyes advanced corneal astigmatism]
- •1. those with one eye having eccentric fixation
- •2. At least one of the following:
- •-those with corneal scarring or who have had corneal surgery including corneal laser surgery
- •-microphthalmos
- •-buphthalmos
- •(except ; In case there is no present symptom at screening time, despite history of dry eye
- •-lid squeezers, blepharospasm
- •-nystagmus
- •-keratoconus
- •-any other corneal or conjunctival pathology of infection
- •3. Wearing contact lenses Within 2 weeks of screening time
- •4. Known hypersensitivity to local anesthetic (ex; proparacaine hydrochloride) and Fluorescent pigment (ex; fluorescein)
- •5. Person who participates in other interventional clinical trials within a period of one month
- •6. Pregnant, breast-feeding, possibly pregnant women
- •7. Ineligible for participating in this study according to the investigator or sub-investigator
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