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临床试验/NCT07693673
NCT07693673已完成不适用

Corneal Topography and High Order Aberrations in Women on Regular Contraceptive Pills

Elshimaa A.Mateen1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2024年10月1日最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
40
试验地点
1
主要终点
Change in Kmax (D)

研究概览

简要总结

Effect of regular usage of contraceptive pills on corneal topography and corneal high-order aberrations

详细描述

Comparing corneal topographic changes and corneal high-order aberrations for women planning to use oral contaceptive pills before and after the usage of the pills

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
18 Years 至 40 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • Female participants aged 18-40 years.
  • Prescribed combined oral contraceptive pills as part of routine gynecological care.
  • Willing to undergo corneal topography/tomography before starting treatment and after 1 year.
  • No previous history of corneal disease or ocular surgery.
  • Able to provide informed consent.

排除标准

  • Keratoconus or suspected corneal ectasia.
  • Corneal opacity, dystrophy, degeneration, or scarring.
  • Previous ocular surgery or significant ocular trauma.
  • Current contact lens use or recent contact lens use without adequate discontinuation period.
  • Active ocular surface disease or severe dry eye.
  • Glaucoma, uveitis, retinal disease, or other significant ocular pathology.
  • Diabetes mellitus, autoimmune disease, thyroid disease, pregnancy, or lactation.
  • Use of other hormonal therapy or systemic medications known to affect corneal parameters.

结局指标

主要结局

Change in Kmax (D)

时间窗: one year

change in corneal thickness (um)

时间窗: one year

Change in K1 (D)

时间窗: Baseline and 1 year

Change in K2 (D)

时间窗: one year

次要结局

未报告次要终点

研究者

发起方
Elshimaa A.Mateen
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Elshimaa A.Mateen

Assistant Professor

Sohag University

研究点 (1)

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