跳至主要内容
临床试验/NCT02876185
NCT02876185已完成不适用

Evaluation of the Possibility to Delegate Glaucoma Surveillance to Orthoptists in Hospital

Fondation Ophtalmologique Adolphe de Rothschild4 个研究点 分布在 1 个国家目标入组 133 人开始时间: 2016年4月8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
133
试验地点
4
主要终点
detection by the orthoptists of an abnormality that would require an anticipated ophthalmologic consultation

研究概览

简要总结

Glaucoma is a progressive optical neuropathy, generally associated with ocular hypertension. The treatment aims to stabilize the visual field deficiencies by lowering the intraocular pressure. Due to the fluctuation of the visual field test and re-test measures, the European recommendations are to obtain 6 visual field tests in 2 years (or one every 4 months) in order to know if the pathology is progressing despite the current treatment (or if the treatment is necessary, in cases of intraocular hypertensions). The lack of ophthalmologists renders the monitoring of a beginning glaucoma, rarely compatible with the present recommendations. It is therefore crucial to evaluate new therapeutic alternatives, when faced to a decreasing medical demography and an increase the patient's needs.

This study should allow to validate the possibility to delegate monitoring tasks to orthoptists during glaucoma surveillance. To organize the delegation of this surveillance to orthoptists would permit a better distribution of the ophthalmologist's activities.

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 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age from 18 years old or more
  • Open-angle glaucoma or ocular hypertension

排除标准

  • Other active ocular pathology
  • Monophthalmic patients
  • Patients requiring a Goldmann visual field exam
  • Opposition of the patient to participate to the trial
  • Pregnant women or breastfeeding
  • Patient under juridical protection
  • Lack of affiliation to social security or universal health coverage

结局指标

主要结局

detection by the orthoptists of an abnormality that would require an anticipated ophthalmologic consultation

时间窗: 20 month of follow-up

次要结局

未报告次要终点

研究者

申办方类型
Network
责任方
Sponsor

研究点 (4)

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