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临床试验/KCT0008161
KCT0008161招募中未知

12-week, multi-center, randomized, human body application test for the efficacy evaluation of rTG-Omega3 in dry eye disease accompanied by Meibomian Gland Dysfunction(MGD).

Taejoon Pharm0 个研究点目标入组 140 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
招募中
发起方
入组人数
140

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 70(Year)(—)
性别
All

入选标准

  • 1. A person who has been diagnosed with Meibomian gland dysfunction (MGD) within 3 months(based on the latest surgery) of undergoing binocular cataract surgery(at least one of the three criteria below is satisfied).
  • 1) During eyelid compression, the discharge of meibomian glands is reduced, showing cloudy, toothpaste-like secretions, or viscous secretions.
  • 2) Two or more Telangiectasia on the edge of the eyelid.
  • 3) Two or more Meibomian Glands Orfices are blocked
  • *Drugs/treatment materials used during cataract surgery are subject to institutional standards.
  • 2 Those with a Tearfilm Break-Up Time (TBUT) of less than 10 seconds
  • 3. A person who agrees to participate in this human body application test before the human body application test begins and prepares a written consent form.

排除标准

  • - Those who are judged to be inappropriate to participate in this human application test under the judgment of nvestigators

研究者

发起方
Taejoon Pharm

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