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临床试验/NCT01159340
NCT01159340已完成不适用

Design Compliance Testing of the Icare One Rebound Tonometer According to the American National Standard ANSI Z80.10-2001 and International Standard ISO 8612.2 for Tonometers

Icare Finland Oy1 个研究点 分布在 1 个国家目标入组 260 人开始时间: 2009年5月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
260
试验地点
1

研究概览

简要总结

The clinical performance of Icare ONE Tonometer TA02 was compared to a Goldmann type applanation tonometer (Haag-Streit). Data was collected according to ANSI Z80.10-2003 (ISO 8612.2) standard. Subjects were eligible for the study if they had no exclusion criteria specified in the ANSI/ISO standard. One eye from 260 subjects was selected for the study. The minimum sample size according to the standard is 150. One eye of each subject was selected for the study by an investigator, based on the history of the patient, results of an external examination of the eye with slit lamp, keratometry readings, and prior knowledge of the intraocular pressure (IOP) range. The Icare ONE Tonometer TA02 in comparison to the reference tonometer (Goldmann type tonometer).

研究设计

研究类型
Observational

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • subjects were eligible for the study if they had no exclusion criteria as specified by the ANSI/ISO standard
  • Subjects were selected according to the following exclusion criteria (as given in ANSI Z80.10-2003 and ISO 8612):
  • subjects with only one functional eye
  • those with one eye having poor or eccentric fixation
  • high corneal astigmatism (i.e. those eyes displaying an oval contact image with the Goldmann tonometer)
  • those with corneal scarring or who have had corneal surgery, including corneal laser surgery
  • microphthalmos
  • buphthalmos
  • contact lens wearers
  • lid squeezers (blepharospasm)
  • nystagmus
  • keratoconus
  • any other corneal or conjunctival pathology or infection

排除标准

  • 未提供

研究者

申办方类型
Industry

研究点 (1)

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