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临床试验/EUCTR2006-003140-27-AT
EUCTR2006-003140-27-AT进行中(未招募)不适用

Effects of non-specific Endothelin-A receptor blockade on ocular blood flow in patients with glaucoma

Department of Clinical Pharmacology0 个研究点目标入组 28 人开始时间: 2006年7月26日最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
进行中(未招募)
发起方
入组人数
28

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • - Men and women aged over 18 years
  • - Normal findings in the medical history and physical examination unless the investigator considers an
  • abnormality to be clinically irrelevant
  • - Inclusion criteria for patients is primary open angle glaucoma defined as pathological optic disc appearance
  • and characteristic visual field loss
  • - Men and women will be included in equal parts
  • - Ametropia of less than 6 diopters and anisometropia of less than 2 diopters
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range

排除标准

  • Exclusion criteria (glaucoma patients)
  • - Abuse of alcoholic beverages, participation in a clinical trial in the 3 weeks preceding the study
  • - Symptoms of a clinically relevant illness in the 3 weeks before the first study day
  • - History or presence of gastrointestinal, liver or kidney disease, or other conditions known to interfere with
  • distribution, metabolism or excretion of study drugs
  • - Blood donation during the previous 3 weeks
  • - Ametropy > 6 dpt
  • - Systemic treatment with, oral antikoagulation, Glibenclamid or vasoactive drugs
  • - History of IOP > 30 (untreated)
  • - Presence of intraocular pathology other than glaucoma
  • - Advanced visual field defect defined as MD >-10
  • - Presence of PEX (pseudoexfoliation) glaucoma and pigment glaucoma
  • - Ophthalmolgical surgery (including argon laser trabeculoplasty (ALT), trabeculectomy, deep sclerectomy)
  • within the last 6 months before the study
  • - Pregnancy
  • - Diabetes mellitus
  • Exclusion criteria (healthy controls)
  • - Abuse of alcoholic beverages, participation in a clinical trial in the 3 weeks preceding the study
  • - Symptoms of a clinically relevant illness in the 3 weeks before the first study day
  • - History or presence of gastrointestinal, liver or kidney disease, or other conditions known to interfere with
  • distribution, metabolism or excretion of study drugs
  • - Blood donation during the previous 3 weeks
  • - Ametropy > 6 dpt
  • - Systemic treatment with oral anticoagulation, Glibenclamid or vasoactive drugs
  • - Pregnancy
  • - Diabetes mellitus

研究者

发起方
Department of Clinical Pharmacology

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