Intalight Reference Database Protocol for VG200D
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 发起方
- 入组人数
- 350
- 试验地点
- 3
- 主要终点
- Quantitative ocular structures
研究概览
简要总结
The goal of this study is to collect OCT scans on normal healthy eyes from an investigational OCT device the VG200D from Intalight, Inc, in order to establish a reference database. The reference database will be used to establish normal ranges for thickness measurement parameters provided by the VG200D OCT software including anterior segment and posterior segment measurements. The study will enroll normal eyes from three clinics in the US including a wide range of ages and races/ethnicities.
详细描述
The goal of this study is to capture VG200D OCT and OCTA scans on at least 350 normal, healthy eyes from individuals with an average age between 55-60 years of age that come from a wide range of ethnicities and races to roughly approximate the US population. This data will be used to create distribution curves for each measurement parameter and to determine the cut-off values at the 1%, 5%, 95% and 99% values for each measurement parameter. Cut-off values will be determined using a non-parametric method based on the distribution directly. Each measurement parameter distribution and associated cut-off values will be used to create a 'Reference Database' that will be used to provide feedback to clinicians using the device. When the user captures a scan on a patient, the software will indicate where a given measurement value falls within this distribution. Values between the 5% and 95% are colored green and labelled 'within normal limits', values between the 1% and 5% and between the 95% and 99% are colored yellow and labelled 'borderline', and values below the 1% and above the 99% are colored red and labelled 'outside normal limits'. These classifications aid the clinician in interpretation of the scan data by providing information where a given patient falls within the Reference Database distribution. These values are based on a comparison to the Reference Database and should be used to aid clinical decisions in combination with other clinical information available, they should not be used as the sole basis for clinical decisions.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Prospective
入排标准
- 年龄范围
- 22 Years 至 —(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •1. Subject 22 years of age or older on the date of informed consent
- •Subject able to understand the written informed consent and willing to participate as evidenced by signing the informed consent
- •Subjects presenting at the site with normal eyes. Cataracts, LASIK, PRK, and peripheral pathology that does not affect the posterior pole region, for example lattice and peripheral drusen, are allowed.
- •4. BCVA 20/40 or better (each eye)
- •Subject is able to comply with the study procedures
排除标准
- •1. Subject unable to tolerate ophthalmic imaging
- •Subject has an ocular pathology other than cataract or mild peripheral, age-related changes (e.g., peripheral drusen, lattice, etc.)
- •Glaucoma diagnosis in either eye.
- •Subject has a condition or is in a situation which the investigator feels may put the subject at significant risk, may confound the study results, or may interfere significantly with the subject's participation in the study
- •Subject with ocular media not sufficiently clear to obtain acceptable OCT images
研究组 & 干预措施
Normal
This group includes subjects with normal healthy eyes as confirmed by a clinical examination by trained eye-care professionals
干预措施: OCT device called VG200D (Device)
结局指标
主要结局
Quantitative ocular structures
时间窗: this study will alst approximately 6 months
Retinal structural measurements of the anterior and posterior segments of the eye
次要结局
未报告次要终点
