NL-OMON46482撤回不适用
Evaluation of non-invasive intracranial pressure technology for use in glaucoma - Non invasive ICP measurement technology in glaucoma
适应症
试验速览
- 阶段
- 不适用
- 状态
- 撤回
- 入组人数
- 60
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
- 18 至 99（—）
入选标准
- •- 50-75 years of age
- •- Presence of DPOAEs and tympanometry in at least one ear
- •- Group 1: Upright IOP of 21mmHg or lower (determined during the screening test)
- •- Group 2: Diagnosed Glaucoma, upright IOP of 21mmHg or lower with or without IOP lowering treatment, and established disease progression rate based on perimetry
- •- Sign the informed consent.
排除标准
- •- Poor condition of both middle ears during the tympanometric test
- •- No presence of DPOAEs
- •- Abnormality of the middle ear or external auditory canal (sequelae of ear infections, cerumen, sequelae of intervention on the tympanic membrane).
- •- For healthy controls, any eye disease or family history of glaucoma. This will be determined by form F1 and the ophthalmologic screening described in section 2 of C1 (reseach protocol).
研究者
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