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临床试验/NCT03581864
NCT03581864已完成不适用

Clinical Outcomes of Implantationof Black Diaphragm Intraocular Lens in Complete Aniridia and Aphakia Due to Posttraumatic Eye Rupture

Medical University of Lublin1 个研究点 分布在 1 个国家目标入组 14 人开始时间: 2006年1月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
14
试验地点
1
主要终点
The medical history

研究概览

简要总结

Purpose: To assess long-term outcomes of implantation of black diaphragmintraocular lens (BD IOL) in postraumatic aniridia and aphakia due to eye rupture.

METHODS: This is retrospective consecutive case series of 14 eyes with post-traumatic complete aniridia and aphakia treated withscleral fixation of BD IOL with. Measurements included ophthalmological comorbidities, best corrected visual acuity (BCVA), complications, and postoperative interventions. The average postoperative follow-up period was 36 months.

研究设计

研究类型
Observational
观察模型
Case Only
时间视角
Retrospective

入排标准

年龄范围
25 Years 至 79 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • post-traumatic complete aniridia and aphakia

排除标准

  • active ocluar inflammation or infection

结局指标

主要结局

The medical history

时间窗: 10 to 120 months

Coexisting eye diseases and post-operative complications were noted.

The slit lamp examination

时间窗: 10 to 120 months

The anterior segment of the eye and eye fundus were examined.

The intrraocular pressure measurement

时间窗: 10 to 120 months

The procedure was performed with the Goldman applanation tonometer.

Best-corrected visual acuity

时间窗: 10 to 120 months

The visual acuity measurement with ETDRS chart

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Dominika Nowakowska

PhD

Medical University of Lublin

研究点 (1)

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