NCT00802269终止4 期
Pain Using Reduced Fluence Parameters in Photocoagulation for Diabetic Retinopathy.
Asociación para Evitar la Ceguera en México1 个研究点 分布在 1 个国家目标入组 25 人开始时间: 2008年3月1日最近更新:
适应症
干预措施
试验速览
- 阶段
- 4 期
- 状态
- 终止
- 发起方
- 入组人数
- 25
- 试验地点
- 1
- 主要终点
- Pain (NRS-11 scale)
研究概览
简要总结
The used of reduced fluence parameters for panretinal photocoagulation decreases pain as perceived by the patient, compared to traditional parameters.
研究设计
- 研究类型
- Interventional
- 分配方式
- Non Randomized
- 干预模型
- Single Group
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 80 Years(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Patients 18 years or older, that signed informed consent
- •Proliferative diabetic retinopathy with indication for panretinal photocoagulation
排除标准
- •Previous retinal photocoagulation
- •Previous ocular surgical procedures
- •Ocular media opacities
- •History of trigeminal neuralgia
- •Chronic ocular pain
- •Depression under conductual or medical treatment
研究组 & 干预措施
Reduced Fluence Parameters
Experimental
Eyes receiving retinal photocoagulation with reduced fluence parameters (time 20-50 msec, power 400-700 mW)
干预措施: Retinal laser photocoagulation (Procedure)
Traditional parameters
Active Comparator
Eyes receiving retinal photocoagulation with traditional parameters (time 100-200 msec, power 200-400 mW)
干预措施: Retinal laser photocoagulation (Procedure)
结局指标
主要结局
Pain (NRS-11 scale)
时间窗: Immediately post-treatment
次要结局
未报告次要终点
研究者
研究点 (1)
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