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临床试验/NCT01663688
NCT01663688
已完成
不适用

Normative Data Collection Study of the Nidek Optical Coherence Tomography RS-3000 for the Measurements of Retinal and RNFL Thickness and Optic Disc Analysis

Nidek Co. LTD.3 个研究点 分布在 1 个国家目标入组 279 人2012年7月

概览

阶段
不适用
干预措施
未指定
疾病 / 适应症
Ocular Physiology
发起方
Nidek Co. LTD.
入组人数
279
试验地点
3
主要终点
Development of age-specific normal ranges for the thickness of the retina and retinal nerve fiber layer (RNFL) and Optic Disc Analysis
状态
已完成
最后更新
12年前

概览

简要总结

The purpose of this clinical study is to collect and evaluate the data from eye scans using an investigational three-dimensional eye imaging photography device called the Nidek Optical Coherence Tomography (OCT) RS-3000. OCT stands for Optical Coherence Tomography, a technique that uses invisible wavelengths of light to make detailed images of the tissues at the back of the eye. These images provide information that physicians may use to help diagnose eye conditions and/or to monitor changes in the eye during treatment.

详细描述

This is a prospective, open-labeled, multi-center clinical study. After qualifying examination of a subject, 3D retinal measurement in the proximity of the optic disc and the macula are carried out for eligible subjects with normal eyes using an investigational three-dimensional eye imaging photography device called the Nidek Optical Coherence Tomography (OCT) RS-3000. The primary objective of this clinical study is to develop age-specific normal ranges for the thickness of the retina and retinal nerve fiber layer (RNFL) etc. using the Nidek Optical Coherence Tomography (OCT) RS-3000 with normative database. The secondary objective is to evaluate any adverse events found during the clinical study.

注册库
clinicaltrials.gov
开始日期
2012年7月
结束日期
2013年8月
最后更新
12年前
研究类型
Observational
性别
All

研究者

发起方
Nidek Co. LTD.
责任方
Sponsor

入排标准

入选标准

  • Normal and healthy male and female subjects at least 20 years of age.
  • Exclusion Criteria
  • Subjects who have extensive or debilitating systemic diseases.
  • Subjects who have significant ocular disease.
  • Subjects who are extremely far sighted or extremely near sighted.

排除标准

  • 未提供

结局指标

主要结局

Development of age-specific normal ranges for the thickness of the retina and retinal nerve fiber layer (RNFL) and Optic Disc Analysis

时间窗: Subjects will be followed for the duration of the procedure, up to one day.

The primary objective of this clinical study is to develop age-specific normal ranges for the thickness of the retina and retinal nerve fiber layer (RNFL)and Optic Disc Analysis.

次要结局

  • Evaluation of adverse events found during the clinical study(Subjects will be followed for the duration of the procedure, up to one day.)

研究点 (3)

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