Postoperative pain management in emergency abdominal surgery: bimodal versus unimodal analgesia
Not Applicable
- Conditions
- Surgery
- Registration Number
- PACTR202103703462058
- Lead Sponsor
- Frank Enoch Gyamfi
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- All
- Target Recruitment
- 108
Inclusion Criteria
Patients between 18 and 80 years of age.
Patients undergoing emergency abdominal surgery
Anticipated abdominal incision of at least 5cm long
Patients who consent to take part in the study
Exclusion Criteria
Patients who are allergic to paracetamol or morphine
Patients with impaired hepatic function or clinical features of liver disease
Patients with renal impairment and CrCl < 60ml/min
Patients with chronic opioid dependence
Patients who are critically ill and may need ICU care
Patients with a neuropsychiatric condition that may impair pain assessment
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method