EUCTR2011-004702-17-IEActive, not recruitingNot Applicable
Comparison of Ultrasound - Guided Continuous Rectus Sheath Blockade and Continuous Preperitoneal Wound Catheter Infiltration of Local Anaesthetic for Postoperative Analgesia following Laparotomy.
Conditions
Drugs
Trial Snapshot
- Phase
- Not Applicable
- Status
- Active, not recruiting
- Sponsor
- Department of Anaesthesia
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional clinical trial of medicinal product
Eligibility Criteria
- Sex
- All
Inclusion Criteria
- •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
Exclusion Criteria
- •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.
Investigators
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