临床试验/NCT00538421

NCT00538421已完成4 期

Opioid-potentiated Volative Anaesthetic(Sevoflurane)Compared to Remifentanil and Propofol During Abdominal Aortic Aneurysm Surgery

Sykehuset i Vestfold HF1 个研究点分布在 1 个国家目标入组 193 人开始时间: 2008年3月最近更新: 2013年3月11日

适应症

干预措施

试验速览

阶段: 4 期
状态: 已完成
发起方: Sykehuset i Vestfold HF
入组人数: 193
试验地点: 1

研究概览研究设计入排标准研究组 & 干预措施研究者研究点记录与标识符相似试验

研究概览

简要总结

Comparing 2 different anaesthetic methods during abdominal aortic aneurysm surgery. The patients will be followed up 30 days postoperative. Number of patients included will be 200. Perioperative details will be analyzed.

研究设计

研究类型: Interventional
分配方式: Randomized
干预模型: Parallel
主要目的: Treatment
盲法: None

入排标准

年龄范围: 18 Years 至 —（Adult, Older Adult）
性别: All
接受健康志愿者: 否

入选标准

•Patients who are planned for open, elective abdominal aortic aneurysm surgery.
•ASA group 1-4.

排除标准

•Patients below 18 years.
•Patients who are included in other pharmaceutical studies.
•Opioids-, benzodiazepins-, antiepileptic drugs-, alcohol- and α2-agonists abuse.
•Pregnant and breastfeeding women.
•Patients with familiar history of malignant hyperthermia.
•Patients with known hypersensitivity for opioids, propofol or volative anaesthetics.
•Patients with considerable arrythmia (atrial fibrillation /atrial flutter is acceptable). Uncontrolled hypertension, serious psychiatric disease.
•Patients with unstable angina pectoris or myocardial infarction last month before inclusion.
•Acute abdominal aortic surgery. Acute dissection or rupture.
•Planned laparoscopic abdominal aortic aneurysm surgery.

研究组 & 干预措施

1

Active Comparator

干预措施: Propofol (Drug)

2

Active Comparator

干预措施: Sevoflurane (Drug)

研究者

发起方

Sykehuset i Vestfold HF

申办方类型

Other

责任方

Principal Investigator

主要研究者

Espen Lindholm

Chief consultant

Sykehuset i Vestfold HF

研究点 (1)

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