NCT01679392已完成不适用
Transversus Abdominis Plane Block: A Placebo-controlled Study in Healthy Volunteers
Hillerod Hospital, Denmark1 个研究点 分布在 1 个国家目标入组 16 人开始时间: 2012年8月最近更新:
适应症
干预措施
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 16
- 试验地点
- 1
- 主要终点
- Cutaneous analgesic distribution
研究概览
简要总结
In this study we investigate the following properties of the transversus abdominis plane block in healthy volunteers:
- Cutaneous analgesic distribution
- Muscular affection
- Reproducibility
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Basic Science
- 盲法
- Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •American society of anesthesiologists classification 1 or 2
- •Written informed consent
排除标准
- •Age below 18 years
- •American society of anesthesiologists classification above 2
- •Body weight below 50 kg
- •Body mass index > 35 kg/m2
- •Previous abdominal surgery
- •Acute or chronic pain
- •Use of pain medication less than 24 h prior to study start
- •Allergy to local anesthetics
- •Pregnancy
- •Breastfeeding
研究组 & 干预措施
Ropivacaine
Experimental
Unilateral transversus abdominis plane block with 20 ml ropivacaine (7.5 mg/ml)
干预措施: Ropivacaine (Drug)
结局指标
主要结局
Cutaneous analgesic distribution
时间窗: 90 min
Cutaneous analgesic distribution 90 min after transversus abdominis plane block administration
次要结局
- Muscular affection of the transversus abdominis plane block(90 min)
- Reproducibility of the transversus abdominis plane block(At least 2 days)
研究者
Kai Henrik Wiborg Lange
Associate Professor
Hillerod Hospital, Denmark
研究点 (1)
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