EUCTR2006-006166-42-DE进行中（未招募）不适用
Exelon bei dementiellem Syndrom bei Patienten mit Progressiver Supranukleärer Parese -offene, prospektive Phase II-Studie
niversity of Tuebingen0 个研究点开始时间: 2007年1月2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
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
- •Inclusion criteria for study participation are:
- •1) definite diagnosis of PSP and dementia
- •2) informed consent to study participation
- •3) MMST > 18, therefore ability to give informed consent
- •4) age over 50 years
- •5) existence of a caregiver who can be suppervise the process of study medication
- •6) ability to communicate verbally
- •7) no other diseases affecting the central nervous system
- •8) adequate capacity for study participation and steady state of health
- •9) ability for consent is controlled by an independent physician
- •10) written consent
- •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
- •1. history of addiction to alcohol or drugs
- •2. signs of psychosis
- •3. former history of ChEI medication
- •4. pregnancy and breast feeding
- •5. history of hypersensitivity aganst rivastigmine
- •6. severe liver insufficiency
- •7. history of sick-sinus-syndrom
- •8. bronchial asthma or obstructiv lung desease
- •9. activ gastric ulcer or duodenal ulcer
- •10. history of retention of urine
- •11. history of convulsion
- •anamnestisch erhobener Alkoholabusus
- •2.akute Psychose
- •3.Einnahme von Cholinesterasehemmern
研究者
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