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临床试验/NCT01054027
NCT01054027已完成不适用

A Randomized Controlled Trial to Determine the Lowest Effective Dose for Adequate Mydriasis in Premature Infants

Georgetown University1 个研究点 分布在 1 个国家目标入组 15 人开始时间: 2007年3月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
15
试验地点
1
主要终点
dilation of the pupil in millimeters

研究概览

简要总结

The purpose of this study is to compare the dilating effect of 0, 1, 2 or 3 drops of mydriatic (pupil dilating) in premature infants undergoing routine retinal (eye) screening exams for Retinopathy of Prematurity (ROP).

详细描述

Premature infants need to have eye exams starting at about 4 weeks of age and continuing until their retinas (membrane at the back of the eye which collects and transfers light) is fully grown. These exams are done to see if they have developed ROP, a disease which can lead to blindness if not treated.

The ophthalmologist (eye doctor) looks through the enlarged pupil (opening at the front of the eye) to see the retina. The drug that is used to dilate the pupil, Cyclomydril, has been shown to have side effects in premature infants. No literature has shown what the optimal dose is for premature babies. Nursery policy is to give 3 drops of Cyclomydril in each eye, at 5 minute intervals, 45-60 minutes before a scheduled eye exam. We sought to reduce the dose without delaying the exam for an under-sized pupil.

In the study, each infant is randomized at the time of the exam to receive either 0, 1 or 2 drops of Cyclomydril in the left eye and 3 drops in the right eye to serve as their own control. The zero-drop group was created to test the contralateral (opposite eye) effect of 3 drops in the right eye. Pupil dilation size is measured using the Colvard pupillometer by a Pediatric Ophthalmologist examiner (G.V.V.) who was not masked to study group assignment.

Measures of pupil size are done at baseline (before any drops given), 45, 90 and 120 minutes after the first drop was given. ROP screening exam is done at the first opportunity to visualize the posterior and peripheral retina.

Additional drops are given at 120 minutes if the observer is unable to complete the exam prior to that point.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Factorial
主要目的
Screening
盲法
None

入排标准

性别
All
接受健康志愿者

入选标准

  • Premature infants undergoing clinically indicated retinal exams

排除标准

  • Ocular congenital anomalies
  • Pre-threshold ROP

研究组 & 干预措施

0 Drop

Experimental

Left eye dose

干预措施: 1% phenylephrine and 0.2% cyclopentolate (Drug)

1 Drop

Experimental

Left eye dose

干预措施: 1% phenylephrine and 0.2% cyclopentolate (Drug)

2 drop

Experimental

Left eye dose

干预措施: 1% phenylephrine and 0.2% cyclopentolate (Drug)

3 drops

Active Comparator

Right eye dose for all groups

干预措施: 1% phenylephrine and 0.2% cyclopentolate (Drug)

结局指标

主要结局

dilation of the pupil in millimeters

时间窗: at baseline (no drops yet instilled), 45, 90 and 120 minutes after drops instilled

次要结局

未报告次要终点

研究者

申办方类型
Other

研究点 (1)

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Study on Effective Mydriasis in Premature Infants | 临床试验