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临床试验/NCT00691925
NCT00691925已完成不适用

Contact Lens for Mitigating Pain Following Refractive Procedure

FORSIGHT Vision31 个研究点 分布在 1 个国家目标入组 4 人开始时间: 2008年6月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
4
试验地点
1

研究概览

简要总结

Using Contact lens following refractive procedure to reduce pain.

详细描述

Patients at day 1 following the procedure will be treated with a contact lens and assessed for pain at 1,2,4 hours and 1,3,5 days.

prospective comparative study

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
18 Years 至 60 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Patients who underwent bilateral Refractive surgery for myopic correction.
  • Evidence of an epithelial defect.
  • Patient complains of significant pain.
  • Patients able to understand the requirements of the study and willing to follow study instructions, to provide written informed consent to participate, and who agree to comply with all study requirements, including the required study follow-up visits.

排除标准

  • Any other anterior segment abnormality other than that associated with Refractive surgery.
  • Any abnormalities associated with the eye lids.
  • Prior laser treatment of the retina.
  • Any ophthalmic surgery performed within three (3) months prior to study excluding Refractive surgery.
  • Diagnosis of glaucoma.
  • Active diabetic retinopathy.
  • Clinically significant inflammation or infection within six (6) months prior to study.
  • Uncontrolled systemic disease (e.g., diabetes, hypertension, etc.) in the opinion of the Investigator.
  • Participation in any study involving an investigational drug within the past 30 calendar days, or ongoing participation in a study with an investigational material.
  • Intolerance or hypersensitivity to topical anesthetics,
  • Specifically known intolerance or hypersensitivity to contact lenses.
  • A medical condition, serious intercurrent illness, or extenuating circumstance that would significantly decrease study compliance, including all prescribed follow-up.
  • Any condition that, in the opinion of the investigator, would jeopardize the safety of the patient.

研究者

发起方
FORSIGHT Vision3
申办方类型
Industry

研究点 (1)

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