CTRI/2023/04/051897尚未招募Unknown
To assess the safety and efficacy of posterior chamber phakic intraocular lens (PCPIOL) in patients with high myopia
试验速览
- 阶段
- Unknown
- 状态
- 尚未招募
- 发起方
- Aurolab
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
入选标准
- •a) Adults of > 21 years
- •b) Stable refraction atleast for 1 year
- •c) Myopia and Myopic astigmatism less than 1 D of corneal astigmatism
- •d) Clear intraocular media
- •e) Intraocular pressure of <20mmHg
- •f) Anterior chamber depth of atleast 2.8 mm and angle <33 degree (from pentacam)
- •g) Endothelial cell count >2500 cells/mm2
- •h) Normal posterior segment
- •i) AS OCT (Open angles)
- •j) Abnormal elevation and curvature maps not fit for corneal refractive surgery.
- •k) understand and willing to participate in the study for 2 years of follow up period
- •l) No systemic illness
排除标准
- •a) Participation in any other drug or device clinical trial within 90 days prior to enrolling in this study and/or during study participation
- •b) corneal pathologic conditions like degenerations and dystrophies and keratoconus
- •c) Evidence of any lens opacity or developing cataract, pseudoexfoliation or pigmentory dispersion
- •d) History of glaucoma and uveitis
- •e) Previous history of ocular diseases
- •f) History of any intraocular or corneal surgery in either eye (including LASIK PRK LRI etc)
- •g) Anterior chamber depth <2.8 mm and angle <33 degree
- •h) Pregnancy and lactation
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