EUCTR2010-024100-10-NL进行中（未招募）1 期
Clonidine as an adjuvant to prolong local anaesthesia in ophthalmic surgery with cryocoagulation. A randomized, controlled, patient-masked trial. - Retrobulbar clonidine
The Rotterdam Eye Hospital0 个研究点目标入组 101 人开始时间: 2010年11月24日最近更新:
适应症
相关药物
试验速览
- 阶段
- 1 期
- 状态
- 进行中（未招募）
- 发起方
- 入组人数
- 101
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
- •- Age = 18 years.
- •- Informed consent.
- •- Rhegmatogenous retinal detachment requiring cryocoagulation and episcleral explant.
- •- Glaucoma requiring cryocoagulation of the ciliary body.
- •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
- •- Hypersensitivity to clonidine or any other ingredients in the product.
- •- Severe bradyarrhythmia as a result of sick sinus syndrome or 2nd or 3rd degree AV block.
- •- Use of oral clonidine.
- •- Cerebrovascular disease, heart failure, coronary insufficiency, occlusive peripheral vascular disorder.
- •- Lapp lactase deficiency or glucose-galactose malabsorption.
- •- Bipolar disorder.
- •- All (other) contraindications and warnings mentioned in the Summary of Product Characteristics of Catapresan.
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