Status:
COMPLETED
Analgesic Efficacy of Intravenous Lidocaine and/or Ketamine
Lead Sponsor:
University of Lausanne Hospitals
Conditions:
Postoperative Pain
Eligibility:
All Genders
20-75 years
Phase:
NA
Brief Summary
The aim of the present study is to evaluate the analgesic benefit of intravenous lidocaine and ketamine in the perioperative period of abdominal surgery.
Detailed Description
Optimal postoperative pain management facilitates rehabilitation immediately after abdominal surgery. Multiple studies have demonstrated that successful postoperative analgesia also reduces perioperat...
Eligibility Criteria
Inclusion
- abdominal surgery by laparotomy
Exclusion
- laparoscopy
- history of chronic pain
- opioid self-administration
- psychiatric disorders
- difficulties with communication
- renal or hepatic dysfunction
- ASA physical status \> 3
Key Trial Info
Start Date :
December 1 2005
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
July 1 2007
Estimated Enrollment :
52 Patients enrolled
Trial Details
Trial ID
NCT01439399
Start Date
December 1 2005
End Date
July 1 2007
Last Update
September 23 2011
Active Locations (1)
Enter a location and click search to find clinical trials sorted by distance.
1
University Hospital Center and University
Lausanne, Canton of Vaud, Switzerland, CH-1011