跳至主要内容
临床试验/NCT01572350
NCT01572350已完成3 期

Randomized Multicenter Clinical Trial of Three Parallel Groups to Estimate the Safety and Efficacy of Triamcinolone Acetonide Combined With Laser, Bevacizumab Combined With Laser Versus Laser Alone for the Treatment of Diffuse Non-tractional Diabetic Macular Edema.

Hospital Universitario de Canarias1 个研究点 分布在 1 个国家目标入组 105 人开始时间: 2010年10月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
状态
已完成
入组人数
105
试验地点
1
主要终点
Best-Corrected Visual Acuity (BCVA)

研究概览

简要总结

This clinical trial is designed to investigate differences in terms of efficacy (mean change in best corrected visual acuity obtained after 12 months of treatment) and safety, of 3 therapeutic estrategies for non-tractional macular edema in diabetic patients: a) laser alone; b) laser plus tiramcinolon; and c) laser plus bevacizumab.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

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

  • 未提供

排除标准

  • 未提供

研究组 & 干预措施

Bevacizumab

Experimental

干预措施: Bevacizumab (Drug)

Grid laser

Active Comparator

It's a reference standard as the treatment which is currently accepted for NTDDME

干预措施: Grid laser (Other)

Triamcinolone 4 mg

Experimental

干预措施: Triamcinolone Acetonide (Drug)

结局指标

主要结局

Best-Corrected Visual Acuity (BCVA)

时间窗: 12 months

To evaluate the effect on best-corrected visual acuity (BCVA) of intravitreal triamcinolone (Triesence ®) or bevacizumab (Avastin ®) in combination with grid laser therapy compared to grid laser therapy alone after 12 months of treatment, in diabetic patients with not tractional diffuse macular edema (NTDDEM)

次要结局

  • To assess the safety of intravitreal Triesence (r)(Baseline, 3m, 6m and 12 months)
  • To measure average change in mean central macular thickness in each group.(Baseline and 3, 6 and 12 months after the treatment was initiated.)
  • To assess the safety of intravitreal Avastin (r)(Baseline, 3m, 6m and 12 months)
  • To assess the safety of intravitreal grid photocoagulation(Baseline, 3m, 6m and 12 months)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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