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
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