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临床试验/ACTRN12618001025224
ACTRN12618001025224已完成4 期

Diurnal Intraocular Pressure Self-monitoring (DIPS) in glaucoma patients on topical medication

Dr. Barbara Zangerl0 个研究点目标入组 19 人开始时间: 2018年6月19日最近更新:
适应症

试验速览

阶段
4 期
状态
已完成
发起方
入组人数
19

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Non-randomised trial
主要目的
Treatment
盲法
Blinded (masking used)

入排标准

年龄范围
18 Years 至 o limit(—)
性别
All

入选标准

  • Group 1: Patients, diagnosed with glaucoma or ocular hypertension who are taking topical medications to reduce intraocular pressure (prostaglandin analogue or beta-blocker)
  • Group 2: Patients, newly with diagnosed glaucoma or ocular hypertension who have been prescribed (but not yet started taking) a topical medication (prostaglandin analogue or beta-blocker) by the attending clinician.

排除标准

  • - Known sensitivity to latanoprost or timolol eye drops
  • - History of breathing problems or pulmonary disease including asthma, chronic obstructive pulmonary disease
  • - History of heart disease involving slowed heart rate, impaired electrical conduction of the heart (i.e. sinus bradycardia, AV block) or chronic heart failure.
  • - Contact lens use
  • - Only one functional eye, poor or eccentric fixation, nystagmus
  • - Any corneal or conjunctival pathology or infection (keratoconus, corneal scarring, severe dry eye disease)
  • - History of prior incisional glaucoma surgery or cornea surgery, including corneal laser surgery
  • - Cataract extraction within the last two months in the study eye(s)
  • - Sensory or functional impairments that may limit self-handling of the ICARE HOME tonometer
  • - Lack of comprehension or willingness to use the tonometer as instructed

研究者

发起方
Dr. Barbara Zangerl

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