EUCTR2011-004702-17-IE
进行中（未招募）
不适用
Comparison of Ultrasound - Guided Continuous Rectus Sheath Blockade and Continuous Preperitoneal Wound Catheter Infiltration of Local Anaesthetic for Postoperative Analgesia following Laparotomy.
适应症This study will involve the continuous infusion of local anaesthetic, into either the rectus sheath space, or the preperitoneal space, in order to achieve optimal analgesia for patients who have undergone a laparotomy. We will compare analgesic efficacy of these techniques over the first 72 hours in the postoperative period.MedDRA version: 14.0Level: LLTClassification code 10036236Term: Postoperative pain reliefSystem Organ Class: 10042613 - Surgical and medical proceduresTherapeutic area: Analytical, Diagnostic and Therapeutic Techniques and Equipment [E] - Anesthesia and Analgesia [E03]
相关药物Chirocaine
概览
- 阶段
- 不适用
- 干预措施
- 未指定
- 疾病 / 适应症
- This study will involve the continuous infusion of local anaesthetic, into either the rectus sheath space, or the preperitoneal space, in order to achieve optimal analgesia for patients who have undergone a laparotomy. We will compare analgesic efficacy of these techniques over the first 72 hours in the postoperative period.
- 发起方
- Department of Anaesthesia
- 状态
- 进行中（未招募）
- 最后更新
- 14年前
概览
简要总结
暂无简介。
研究者
入排标准
入选标准
- •Adult general surgical patients presenting for laparotomy
- •Written informed consent
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1\.2 Adults (18\-64 years) yes
- •F.1\.2\.1 Number of subjects for this age range 60
- •F.1\.3 Elderly (\>\=65 years) yes
- •F.1\.3\.1 Number of subjects for this age range 60
排除标准
- •Patient refusal.
- •Local infection at site of insertion.
- •Allergy to amide local anaesthetics, opioids, paracetamol, NSAIDs, ketamine, NMBs, volatile anaesthetics.
- •Concurrent use of antiarrhythmics with local anaesthetic activity.
- •Concurrent use of MAOIs or within 2 weeks of MAOI use.
- •Severe liver or cardiac dysfunction.
- •Inability to comprehend pain scoring system.
- •Elderly or debilitated patients that require a reduction in levobupivacaine dose commensurate with their physical status, resulting in the protocol not being followed.
结局指标
主要结局
未指定
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