跳至主要内容
临床试验/NCT00802269
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

发起方
Asociación para Evitar la Ceguera en México
申办方类型
Other
责任方
Sponsor

研究点 (1)

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