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临床试验/ACTRN12621000075886
ACTRN12621000075886已完成3 期

The effect of 0.05% atropine sulfate eye drops on the binocular vision characteristics of young adult myopes' eyes

Queensland University of Technology0 个研究点目标入组 20 人开始时间: 2021年1月29日最近更新:

试验速览

阶段
3 期
状态
已完成
入组人数
20

研究概览

简要总结

Short-sightedness (myopia) is associated with unstable binocular vision (the way the eyes aim and focus together). Atropine is an eye drop medication which is commonly used to slow short-sightedness progression in very dilute concentrations, where the known medication side effect of reduced focusing ability is thought to be minimised. Few studies have examined the effect of atropine on binocular vision beyond the loss of focusing ability. This research examined the effect of 0.05% atropine eye drops on the aiming and focusing systems of the eyes across a 10-day period. On average, the group receiving atropine had a significant change in the way their eyes aimed at near targets (near heterophoria), and a reduction in their ability to keep this change controlled (negative fusional reserves) compared to the control group. Consistent with previous reports, the group receiving atropine had a significant reduction in their focusing ability, which was reflected in significant changes in a number of parameters, such as decreased accommodative amplitude, binocular accommodative facility, positive relative accommodation; and increased accommodative lag. The control group had no change in any parameter tested.

研究设计

研究类型
Interventional
分配方式
Randomised controlled trial
主要目的
Treatment
盲法
Blinded (masking used)

入排标准

年龄范围
18 Years 至 25 Years(—)
性别
All

入选标准

  • Healthy, young adult myopes with a myopic refractive error between -0.75 and -6.00 DS, with no more than 1.50 DC of astigmatism or 2 D of anisometropia, whose refractive error is currently corrected with single vision distance spectacles or contact lenses, and who have stereoacuity of 200 seconds of arc or greater.

排除标准

  • No current or previous myopia control (atropine, OrthoK, peripheral defocus soft CLs)
  • No amblyopia or strabismus
  • Best corrected visual acuity (BCVA) greater than or equal to 0.1 logMAR, with no more than 1 line difference in VA between eyes
  • Habitual correction (either single vision distance spectacles or contact lenses) within 0.50D of cycloplegic refraction result
  • No pregnancy or breastfeeding
  • No history of ocular surgery
  • No history of significant ocular infection or injury
  • No allergy to atropine, tropicamide, or benzalkonium chloride (BAK)
  • No known angle closure glaucoma, or temporal VH ratio less than 0.3:1 in either eye
  • Intraocular pressure of less than 21 mmHg in each eye
  • No current use of: anticholinergics, antiglaucoma medications, antimyasthenics, potassium drugs, carbachol/physostigmine/pilocarpine, no CNS depressants (such as antiemetics, phenothiazines, or barbiturates).

研究者

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