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临床试验/NCT03613233
NCT03613233Unknown不适用

Quality of Life Assessment in Traditional and Microinvasive Glaucoma Surgery.

Military Institute od Medicine National Research Institute2 个研究点 分布在 1 个国家目标入组 400 人开始时间: 2018年1月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
发起方
入组人数
400
试验地点
2
主要终点
NEI VFQ 25 quality of life score change

研究概览

简要总结

Quality of Life assessment before and after various glaucoma surgery (traditional and microinvasive (MIGS)).

详细描述

Patients qualified for glaucoma surgical procedure fill in QoL questionnaire (NEI VFQ 25) at baseline (pre-operatively) and 3 months after glaucoma surgery. Additional data will be collected such as demographic data and medical data, visual acuity, intraocular pressure, number of glaucoma medications, stage of glaucoma based on visual field assessment, medical ophthalmic history, intra and postoperative complications, postoperative interventions.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
None

入排标准

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

入选标准

  • patients qualified for glaucoma surgery in Military Institute of Medicine - based on following Inclusion Criteria:
  • all glaucoma types with characteristic glaucoma changes (biomicroscopic ,visual field) with documented glaucoma progression
  • patients not tolerating antiglaucoma medications,
  • patients with poor compliance
  • progression in visual field

排除标准

  • active inflammatory disease
  • pregnancy
  • mental disease or emotional instability
  • general steroid therapy
  • inability to fill in the questionnaire

研究组 & 干预措施

traditional glaucoma surgery

Active Comparator

glaucoma procedures such as trabeculectomy, iridencleisis, non - penetrating deep sclerectomy

干预措施: Glaucoma surgery (Procedure)

microinvasive glaucoma surgery (MIGS)

Active Comparator

glaucoma procedures such as : canaloplasty (traditional, ABiC, modified), iStent, XEN, Cypass,Hydrus- and with any other microinvasive IOP reducing device

干预措施: Glaucoma surgery (Procedure)

结局指标

主要结局

NEI VFQ 25 quality of life score change

时间窗: baseline (0-30 days; pre-operative) and three months after surgery

NEI VFQ 25 baseline and 3 months after surgery

次要结局

未报告次要终点

研究者

发起方
Military Institute od Medicine National Research Institute
申办方类型
Other
责任方
Principal Investigator
主要研究者

Marek Rekas

płk prof. Marek RĘKAS, MD, PhD

Military Institute od Medicine National Research Institute

研究点 (2)

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