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临床试验/NCT00597181
NCT00597181终止4 期

A Clinical Study Comparing the Inflammatory Response of the Ex-Press Mini Glaucoma Shunt to Trabeculectomy in Subjects With Open-Angle Glaucoma

Indiana University1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2007年11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
入组人数
40
试验地点
1
主要终点
Aqueous humor flare

研究概览

简要总结

The less invasive nature of the Ex-Press Mini shunt with mitomycin C induces less post-operative inflammation than trabeculectomy with mitomycin c.

详细描述

The purpose of this study is to quantify the degree of post-operative inflammation in eyes which have undergone either trabeculectomy filtering surgery or Ex-Press mini shunt insertion. Early intraocular pressure control and postoperative complications will also be noted.

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
否

入选标准

  • •All subjects must:
  • •Be willing and able to provide written Informed Consent.
  • •Be able and willing to follow instructions on the use of post- operative medication and likely to complete the entire course of the study.
  • •Be male or female of any race at least 18 years of age.
  • •Have medically uncontrolled glaucoma for which they have elected to undergo surgery.
  • •Diagnosed with primary open angle glaucoma, pigmentary or pseudoexfoliation glaucoma.

排除标准

  • •No subject may:
  • •Have any contraindication to intraocular surgery.
  • •Diagnosed with: primary angle closure glaucoma, normal tension glaucoma, secondary glaucoma, neovascular glaucoma.
  • •Have any active ocular disease other than glaucoma that would interfere with study parameters (such as: uveitis, ocular infection, or severe dry eye). Subjects with mild chronic blepharitis, age-related macular degeneration and background diabetic retinopathy may be enrolled at the discretion of the investigator.
  • •Have laser ALT or SLT within the past 3 months or cataract surgery within the last six months.
  • •Require use of ocular NSAID or systemic steroids.
  • •Have known allergy or sensitivity to mitomycin C
  • •Have corneal abnormalities that would interfere with the ability to obtain an adequate laser flare measurement.
  • •Be concurrently enrolled in an investigational drug or device study or participation within the last 30 days in any investigational drug or device study.
  • •Be pregnant, nursing, planning a pregnancy, or be of childbearing potential and not using a reliable form of contraception (a woman is considered of childbearing potential unless she is postmenopausal, has had a uterus and/or both ovaries removed, or has had a bilateral tubal ligation).
  • •Have a situation or condition that in the investigator's opinion may put the subject at significant risk, may confound the study results, or may interfere significantly with participation in the study.

研究组 & 干预措施

1

Active Comparator

Trabeculectomy with Mitomycin C 0.2 mg/cc for 2 minutes

干预措施: Trabeculectomy with mitomycin c (Procedure)

2

Active Comparator

Ex-Press mini shunt; Model R50 with mitomycin C 0.2 mg/cc for 2 minutes

干预措施: Ex-Press mini shunt with mitomycin c (Procedure)

结局指标

主要结局

Aqueous humor flare

时间窗: 2 months

次要结局

  • Aqueous humor cell(2 months)

研究者

申办方类型
Other

研究点 (1)

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