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临床试验/NCT00094744
NCT00094744已完成3 期

A Randomized Trial Comparing Part-time Versus Full-time Patching for Severe Amblyopia

Jaeb Center for Health Research1 个研究点 分布在 1 个国家目标入组 175 人开始时间: 2001年5月1日最近更新:
适应症
干预措施

试验速览

阶段
3 期
状态
已完成
发起方
入组人数
175
试验地点
1
主要终点
Visual acuity improvement at 17wks.

研究概览

简要总结

The goals of this study are:

  • To determine whether the visual acuity improvement obtained with part-time (6 hours) patching is equivalent to the visual acuity improvement obtained with full-time patching (all or all but one waking hour) for severe amblyopia.
  • To develop more precise estimates than currently available for the visual acuity improvement that occurs during treatment of amblyopia with patching.
  • To identify factors that may be associated with successful treatment of amblyopia with patching.

详细描述

Amblyopia is the most common cause of monocular visual impairment in both children and young and middle-aged adults. Patching has been the mainstay of amblyopia therapy. It is generally held that the response to treatment is best when it is instituted at an early age, particularly by age two or three, and is poor when attempted after eight years of age.

For severe amblyopia, it is generally accepted that occlusion with patching is the standard of care. Other modalities of treatment, such as atropine penalization and optical penalization, are widely considered insufficient as initial treatments for severe amblyopia. However, controversy exists with regard to how many hours per day of patching should be prescribed. Advocates of full-time patching purport that such a regimen is needed to restore visual acuity more rapidly and more effectively. Advocates of part-time patching believe it to be better tolerated by the child and family, therefore producing less stress on the parent-child relationship and producing better results through better compliance. Part-time patching may also promote the development of binocularity in patients who have "straight-eyes", reduce the chance of a straight-eyed patient developing manifest strabismus or losing stereopsis, and reduce the incidence of reverse- or occlusion-amblyopia.

The study is a randomized trial comparing daily patching regimes for children with severe amblyopia. It will consist of about 160 children. Patients in the severe (20/100 to 20/400) group will patch part-time (6 hours) or full-time (all or all but one waking hour) of each day for the 4 month study period. There are at least two follow up visits during the 4-month period. Visual acuity is the major study outcome. It is assessed at the 4-month exam.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Outcomes Assessor)

入排标准

年龄范围
3 Years 至 7 Years(Child)
性别
All
接受健康志愿者
否

入选标准

  • •Patients must be less than 7 years of age with the original cause of amblyopia as strabismus or anisometropia (a refractive error difference of more than one diopter between the two eyes.)
  • •Visual acuity in the amblyopic eye must be between 20/100 and 20/
  • •Visual acuity in the sound eye of 20/40 or better.
  • •There must be at least 3 lines of acuity difference between the two eyes.

排除标准

  • •Patching treatment (other than spectacles) within six months prior to enrollment and other amblyopia treatment of any type used within one month prior to enrollment.

研究组 & 干预措施

6hrs daily patching

Active Comparator

6 hours per day of patching in the sound eye

干预措施: Eye patch (Device)

Full-time daily patching

Active Comparator

Patching of the sound eye all but one waking hour

干预措施: Eye patch (Device)

结局指标

主要结局

Visual acuity improvement at 17wks.

时间窗: 17 weeks

次要结局

未报告次要终点

研究者

发起方
Jaeb Center for Health Research
申办方类型
Other

研究点 (1)

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