JPRN-UMIN000013243已完成未知
Efficacy and safety of ExPress glaucoma filtration surgery in normal tension glaucoma - Effect of ExPress glaucoma filtration surgery in NTG
Alcon Japan0 个研究点目标入组 32 人开始时间: 2014年2月24日最近更新:
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 32
研究概览
简要总结
The mean IOP decreased from 14.8+/-2.3 mmHg at baseline to 10.0+/-3.1 mmHg at 12 months after surgery (P<0.0001). IOP reductions>20% were achieved by 61.5% of the eyes at 12 months. Adverse events were typical for filtration procedures, and none was deemed device-related. The mean corneal endothelial cell density had decreased by 3.3% at 12 months after surgery.
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 20years-old 至 ot applicable（—）
- 性别
- All
入选标准
- 未提供
排除标准
- •1. pregnant and nursing women, and woman desiring future fertility during the study period 2. angle closure and secondary glaucoma 3. subject with a history of glaucoma surgery 4. subject to receive or has received penetrating keratoprasty 5. subject to have a problem for the IOP measurement with GAT 6. diagnosed as corneal dystrophy 7. subject with a history of any ocular surgery within 6 months 8. subject with infectious or non-infectious conjunctivitis, keratitis, or uveitis in one or both eyes 9. diagnosed as severe blepharitis or dry eye 10. subject with a metal allergy 11. judged as inappropriate for study subject 12. subject attended to the other clinical trial or study within 30 days before baseline visit
研究者
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