跳至主要内容
临床试验/JPRN-jRCTs032220339
JPRN-jRCTs032220339进行中(未招募)2 期

Repeated low-level red-light therapy for shortening axial length in high myopia children and teenagers:a prospective, single-arm study - Repeated low-level red-light therapy shortens axial length

Ohno Kyoko0 个研究点目标入组 30 人开始时间: 2022年9月20日最近更新:
适应症

试验速览

阶段
2 期
状态
进行中(未招募)
发起方
入组人数
30

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
>= 8age old 至 <= 18age 11month 4weeks old(—)
性别
All

入选标准

  • Provision of consent
  • Age 8 years or older and less than or equal to 18 years old or younger at enrollment. High myopia cycloplegic sphere less than or equal to -6.00 dioptres in both eyes. Willing and able to participate in all required activities of the study. Normal Fundus , tessellated fundus or with peripapillary diffuse chorioretinal atrophy

排除标准

  • The children undergoing or previously treated with myopia control treatments, eg orthokeratology, low dose atropine eye drops, multifocal soft contact lenses. However, children currently using only low dose atropine eye drops, can be recruited but atropine treatment should be discontinued for at least 2 weeks.
  • Secondary myopia, such as a history of retinopathy of prematurity or neonatal problems, or syndromic myopia with a known genetic disease or connective tissue disorders, such as Stickler or Marfan syndrome.
  • Pathologic myopia with signs of macula involving diffuse chorioretinal atrophy, patchy chorioretinal atrophy, macular atrophy, lacquer cracks, myopic choroidal neovascularization or Fuchs spots.
  • Strabismus and binocular vision abnormalities in either eye.
  • Previous Any intraocular surgery affecting refractive status.
  • Other reasons, including but not limited to ocular or other systemic abnormalities, that the physician may consider inappropriate for enrollment.

研究者

发起方
Ohno Kyoko

相似试验