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临床试验/ITMCTR2100004611
ITMCTR2100004611尚未招募未知

A randomized controlled clinical trial study protocol of Bujing Yishi tablet in the treatment of Children and Adolescents with Low-grade Myopia

Affiliated Hospital of Chengdu University of Traditional Chinese Medicine0 个研究点开始时间: 待定最近更新:
适应症

试验速览

阶段
未知
状态
尚未招募
发起方

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional study

入排标准

年龄范围
6 至 12(—)
性别
All

入选标准

  • 1. Meet the diagnostic criteria for myopia;
  • 2. Aged 6 to 12 years;
  • 3. The naked eye vision is below 1.0, and the myopia degree is -0.50D~3.00D;
  • 4. Participants and their guardians with the ability to understand, and write research-related materials, and voluntarily comply with all test requirements;
  • 5. Agree to sign an informed consent form and voluntarily participate in the research.

排除标准

  • 1. Participants with myopia and amblyopia / strabismus;
  • 2. Spherical equivalent (SE)<-0.5D, or combined with pathologic myopia-related fundus changes and/or obvious visual dysfunction;
  • 3. Subjects suffering from serious systemic diseases, such as cerebrovascular, liver, kidney, hematopoietic system, and psychiatric diseases;
  • 4. use other related drugs or treatments within 2 weeks;
  • 5. Participate in other clinical trial research;
  • 6. Allergies to test drugs;
  • 7. Incomplete understanding of the research, refusal to participate or lack of signed informed consent;

研究者

发起方
Affiliated Hospital of Chengdu University of Traditional Chinese Medicine

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