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临床试验/NCT00804921
NCT00804921已完成2 期

Effectiveness of Oral Acetazolamide, Brimonidine Tartarate, and Anterior Chamber Paracentesis for Ocular Hypertension Control After Intravitreal Bevacizumab Injection: Preliminary Results

University of Sao Paulo1 个研究点 分布在 1 个国家开始时间: 2008年12月9日最近更新:
适应症
相关药物

试验速览

阶段
2 期
状态
已完成
试验地点
1
主要终点
Intra-ocular pressure variation after intra-vitreous injection of bevacizumab

研究概览

简要总结

Purpose: To evaluate the effects of anterior chamber paracentesis, brimonidine and oral acetazolamide to reduce intra-ocular pressure (IOP) variations after intravitreal bevacizumab injection (IVBV).

Methods: 47 patients scheduled for IVBV (1.5 mg / 0.06 ml) will be randomly assigned to a pre-treatment 1 hour before IVBV with either 250 mg oral acetazolamide (DIA, 9 eyes), anterior chamber paracentesis immediate after IVBV (PAR, 15 eyes), topic brimonidine tartarate 1 hour before IVBV (BRI, 14 eyes), or no pre-treatment IBVB (CTR, 9 eyes). IOP will be measured 90 minutes before injection (baseline), just before injection, and at 3, 10, 20 and 30 minutes after the procedure.

研究设计

研究类型
Interventional

入排标准

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

入选标准

  • •macular edema

排除标准

  • •pulmonary chronic problems
  • •chronic renal failure
  • •intraocular inflammation
  • •drug or alcohol addiction

结局指标

主要结局

Intra-ocular pressure variation after intra-vitreous injection of bevacizumab

次要结局

未报告次要终点

研究者

申办方类型
Other

研究点 (1)

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