ACTRN12608000291381
Completed
Phase 2
The Analgesic Efficacy of Ultrasound Guided Transversus Abdominis Plane Ropivacaine Continuous Blockade in Patients Undergoing Abdominal Surgery - Pilot Trial
Overview
- Phase
- Phase 2
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- Western Health
- Enrollment
- 20
- Status
- Completed
- Last Updated
- 6 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Age over 18 years
- •Elective or semi\-elective abdominal surgery requiring mid\-line incision
Exclusion Criteria
- •Patient refusal Acute abdomen A clinical history consistent with opioid tolerance including preoperative opioid consumption of longer than one week, intravenous opioid drug use Preoperative use of opioid antagonists like buprenorphine and naltrexone A clinical history of chronic pain, where patients may benefit from early commencement of agents like ketamine Renal impairment with creatinine clearance less than 60 mL/min Drug allergy or contraindication to morphine, ropivacaine, paracetamol Anaesthetist preference for placement of central neuroaxial blockade/catheter Surgeon refusal to placement of catheters Inability of patient to use patient controlled analgesia pump post\-operatively or to understand grading of pain via verbal pain score, laparoscopic assisted surgery
Outcomes
Primary Outcomes
Not specified
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