ACTRN12623001347651
Not yet recruiting
Phase 4
Determine whether analgesia for patients undergoing minimally invasive major abdominal surgery using Intrathecal Morphine with local anaesthetic affects quality of recovery. The AIM Study.
Overview
- Phase
- Phase 4
- Intervention
- Not specified
- Conditions
- Anaesthesiology
- Sponsor
- Alfred Health
- Enrollment
- 280
- Status
- Not yet recruiting
- Last Updated
- 2 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Greater than or equal to 18 years old
- •Patients scheduled for elective major laparoscopic, lap\-assisted or robotic abdominal surgery, and
- •Major surgery is that with a planned operative time of over 2 hours
Exclusion Criteria
- •\< 18 years old
- •Patient declines enrolment or inability to consent
- •Contraindication to intrathecal morphine
- •Contraindication to a neuraxial injection, including; injection site concerns, coagulopathy (including administration of anticoagulant), or untreated sepsis
- •Cognitive impairment or language proficiency leading to inability to complete QoR\-15 questionnaire or understand the pain scores
- •Chronic pain, including baseline opioid use prior to hospital admission
Outcomes
Primary Outcomes
Not specified
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