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临床试验/NCT00801905
NCT00801905终止2 期

Effect of Topical Nepafenac in Macular Thickening Related to Pan-retinal Photocoagulation

Asociación para Evitar la Ceguera en México2 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2008年8月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
终止
发起方
入组人数
50
试验地点
2
主要终点
Central macular thickening

研究概览

简要总结

The purpose of this study is to determine whether topical nepafenac (qid) is effective in preventing and treating macular thickening related pan-retinal photocoagulation in patients with diabetic retinopathy.

详细描述

Objective

To evaluate the effect of topical nepafenac 0.1 %, in preventing and in treating macular thickening related to pan-retinal photocoagulation in diabetic patients. Material and methods: This is a prospective, longitudinal, and controlled study in patients with diabetic retinopathy (severe non-proliferative and proliferative retinopathy), with a symmetric severity in both eyes and without a clinical significant macular edema. The best corrected visual acuity (BCVA) in all patients was 20/80 or better. All patients will undergo pan-retinal photocoagulation in three different sessions (with 2 weeks in apart between them). Each patient will receive topical nepafenac 0.1% (qid) on one eye, and placebo (qid) at the fellow eye, starting 1 week before the first retinal photocoagulation session and continued for 9 weeks ( ending 4 weeks after pan-retinal photocoagulation is completed). Spectral domain OCT and BCVA in ETDRS scale will be performed before and at 2 weeks after each laser session, and at 1, 2 and 3 months after treatment completed. BCVA and OCT outcomes of each studied period will be compared on both eyes, and side effects will be recorded.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Single (Participant)

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients with Severe and proliferative Diabetic Retinopathy
  • Symmetric severity grade on both eyes
  • Best corrected visual acuity better than 20/80

排除标准

  • Clinical significant macular edema
  • Lens opacity
  • Ocular surgery 6 months or less before recruit
  • Uveitis history
  • Actual use of topical or systemic non-steroidal anti inflammatory agents
  • Actual or history of other macular diseases
  • Ocular surface diseases
  • Vitreomacular traction syndrome
  • Other vascular retinal diseases different to diabetic retinopathy
  • Actual or history of use of topical prostaglandin analogues

研究组 & 干预措施

1: Nepafenac

Active Comparator

Topical nepafenac 0.1% is administrated every 6 hour 1 week before start pan-retinal photocoagulation and 4 weeks during all laser session performed biweekly, and 4 weeks after last laser sessión was completed.

干预措施: Nepafenac (Drug)

2: placebo

Placebo Comparator

Topical lubricating is administrated every 6 hours at fellow eye 1 week before start pan-retinal photocoagulation, 4 weeks during each laser session performed biweekly, and 4 weeks after last laser sessión was completed

干预措施: Lubricant (Other)

结局指标

主要结局

Central macular thickening

时间窗: 2 weeks after each laser session and 1 and 2 months after last laser session

次要结局

  • Best corrected visual acuity(2 weeks after each laser session, 1, 2 and 3 months after pan-retinal photocoagulation is completed)

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 (2)

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