CTRI/2024/02/062688招募中4 期
Prospective, single arm, post-marketing clinical study of EYECRYL™PLUS (600) intraocular lens to assess performance and safety in patientsundergoing cataract surgery. - NI
Biotech vision care pvt ltd0 个研究点目标入组 0 人开始时间: 待定最近更新:
试验速览
- 阶段
- 4 期
- 状态
- 招募中
- 发起方
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
- •1. Age 18 year or greater
- •2. Cataract
- •3. Calculated IOL power is within the range of the
- •investigational IOL.
- •4. Clear intraocular media other than cataract
- •5. Patient willing to participate and sign informed consent to
- •participate in study and to use device related data for
- •scientific purpose
- •6. Patient willing to come for all post-operative follow-up
- •7. Female participants of child bearing potential and male
- •participants whose partner is of child bearing potential must
- •be willing to ensure that they or their partner use effective
- •contraception during the study.
排除标准
- •1. Previous intraocular or corneal surgery
- •2. Traumatic cataract
- •3. Pregnancy
- •5. Vulnerable subject.
- •6. Patients receiving chloroquine treatment.
- •7. Patient having Microphthalmia.
- •8. Patient having Chronic Uveitis.
- •9. Patient suffering from corneal dystrophy or endothelial
- •insufficiency.
- •10. Patient having active ocular diseases (active diabetic
- •retinopathy, uncontrolled glaucoma
研究者
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