NL-OMON51638招募中不适用
Study on test-REtest reliability in Patients with inheritEd retinAl dysTrophies (REPEAT study) - REPEAT study
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 入组人数
- 50
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Observational
入排标准
- 年龄范围
- 16 至 99（—）
入选标准
- •In order to be eligible to participate in this study as a visually-impaired
- •patient, a subject must meet all of the following criteria:
- •Willing and able to provide informed consent (IC) for the participation in
- •Minimum age of 16 years;
- •Clinical diagnosis of IRD with BCVA using ETDRS of >=20/50 Snellen equivalent;
- •Willing and able to undergo ophthalmic examinations at two separate occasions;
- •No ocular or non-ocular disease/disorder that may influence the results of
- •the measurements.
- •In order to be eligible to participate in this study as a low-vision patient, a
- •subject must meet all of the following criteria:
- •Willing and able to provide informed consent (IC) for the participation in
- •Minimum age of 16 years;
- •Clinical diagnosis of IRD with BCVA using ETDRS of <20/50 Snellen equivalent;
- •Willing and able to undergo ophthalmic examinations at two separate occasions;
- •No ocular or non-ocular disease/disorder that may influence the results of
- •the measurements
排除标准
- •A potential subject who meets any of the following criteria will be excluded
- •from participation in this study:
- •The last measured BCVA in the better-seeing eye is light-perception;
- •(History of) ocular of non-ocular disease/disorder that may influence the
- •results of the measurements (e.g. amblyopia);
- •Known allergy or intolerance for ocular anesthetic eye drops oxybuprocaine
- •0.4% or mydriatics tropicamide 0.5% and/or phenylephrine 5%;
- •Participation in another research study involving an investigational
- •medicinal product related to their ocular health.
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