CTIS2024-511018-18-00进行中（未招募）1 期
Prospective comparative randomized study of procedural sedation during TAVR (Transcatheter Aortic Valve Replacement)
Azienda Socio Sanitaria Territoriale Ovest Milanese0 个研究点目标入组 1 人开始时间: 2024年3月14日最近更新:
适应症
试验速览
- 阶段
- 1 期
- 状态
- 进行中（未招募）
- 发起方
- 入组人数
- 1
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 65+（—）
- 性别
- All
入选标准
- •Patients undergoing TAVR, Age between 18 and 95 years., Patient's agreement to participate in the protocol and to sign the informed consent form.
排除标准
- •Lack of informed consent, Acute cerebrovascular conditions;, Advanced heart failure., allergies to sedative medications used or to any of the excipients, presence of preoperative delirium, Patients with psychiatric disorders on pharmacological therapy;, Participation in a clinical study where an experimental drug has been administered within 30 days of screening or within the 5 half-lives of the investigational drug (whichever period is longer), Women of potentially childbearing age (potentially childbearing age: any woman who has had her first menstruation until the post-menopausal period; postmenopausal woman: woman at least 45 years old who has not had menstrual periods for at least 12 months);, Concomitant procedures other than TAVR (e.g., Percutaneous Coronary Intervention);, Advanced 2nd or 3rd degree atrioventricular block in patients without a pacemaker;, Uncontrolled hypotension
研究者
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