跳至主要内容
临床试验/NCT00029185
NCT00029185已完成不适用

Topical Dehydrex in Treating Recurrent Corneal Erosion

Holles Laboratories, Inc.2 个研究点 分布在 1 个国家目标入组 300 人开始时间: 2001年9月最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
300
试验地点
2

研究概览

简要总结

This is a compassionate-use treatment study to provide Dehydrex to patients with corneal erosion syndrome who have previously used Dehydrex.

详细描述

This study continues to provide Dehydrex to patients who have received it previously under other studies. Patients continue to be treated with their current dose of Dehydrex. Upward dose adjustments may be made as clinically indicated. Patients undergo eye exams every 3 to 4 months or more often. Downward dose titration will be attempted in patients who are stable, free of symptoms, and willing to attempt downward adjustments. In patients who are able to discontinue the medication, duration of healing will be determined. In those patients who experience a recurrence after discontinuing the medication, Dehydrex will be restarted at a dose higher than the minimum effective dose. After at least 8 weeks of treatment and resolution of symptoms, the dose may again be reduced. Further attempts to discontinue the medication will not be made.

Completion date provided represents the completion date of the grant per OOPD records

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Single Group
主要目的
Treatment
盲法
Double

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

  • 未提供

排除标准

  • 未提供

研究者

申办方类型
Industry

研究点 (2)

Loading locations...

相似试验

Study of Dehydrex in Patients With Corneal Erosion | 临床试验