NCT01999296Unknown不适用
Prospective Evaluation of the Use of Thunderbeat Vessel Sealing Device in Laparoscopic Surgery
Cantonal Hosptal, Baselland1 个研究点 分布在 1 个国家目标入组 250 人开始时间: 2013年10月最近更新:
适应症
试验速览
- 阶段
- 不适用
- 发起方
- 入组人数
- 250
- 试验地点
- 1
- 主要终点
- Use of additional vessel sealing devices
研究概览
简要总结
All patients undergoing laparoscopic visceral and gynecologic procedures using the combined bipolar and ultrasonic vessel sealing and dissection device Thunderbeat are entered in a prospective registry. Data will be analysed concerning the safe use of the instrument and perioperative blood loss.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Prospective
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
- •all patients undergoing laparoscopic visceral or gynecologic surgery
- •need for a vessel sealing device during surgery
排除标准
- •non able to understand informed consent or missing consent
结局指标
主要结局
Use of additional vessel sealing devices
时间窗: one day
Intra- and postoperative device-related complications
时间窗: 30 days
次要结局
- Duration of Surgery(one day)
- Perioperative Blood Loss(30 days)
研究者
Daniel Steinemann, MD
Principal Investigator
Cantonal Hosptal, Baselland
研究点 (1)
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