NL-OMON44659已完成3 期
Dexmedetomidine versus propofol in the awake implantation of a neuromodulative system. - DexMedPro
适应症
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 入组人数
- 72
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 18 至 99（—）
入选标准
- •- Patients need to be between 18 and 65 years.
- •- Patients have an indication for implantation of a neuromodulative system.
排除标准
- •- Hypersensitivity of active part of one of any of the excipients
- •- AV-blok (II or III)
- •- Acute cerebrovascular disease
- •- Pregnancy
- •- Acute epilepsy
- •- Severe liver dysfunction
- •- Use of a beta blocker
- •- Use of medications causing hypotension or bradycardia.
- •- Psychologically unstable
- •- Communication problem
- •- Heart rate <60bpm
- •- Allergy for soya or peanuts
- •- Heart failure
- •- Severe heart disease
- •- Electroconvulsive therapy (ECT)
- •- ASA III, IV, V
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