CompletedN/Aketamine
Analgesic Efficacy of Intravenous Lidocaine and/or Ketamine
Sponsored by University of Lausanne Hospitals
NCT ID
NCT01439399
Target Enrollment
52 participants
Start Date
2005-12
Est. Completion
2007-07
About This Study
The aim of the present study is to evaluate the analgesic benefit of intravenous lidocaine and ketamine in the perioperative period of abdominal surgery.
Conditions Studied
Interventions
- •Lidocaine,
- •Ketamine
- •association ketamine-lidocaine
- •Placebo
Eligibility
Age:20 Years - 75 Years
Healthy Volunteers:No
View full eligibility criteria
Inclusion Criteria: * abdominal surgery by laparotomy Exclusion Criteria: * laparoscopy * history of chronic pain * opioid self-administration * psychiatric disorders * difficulties with communication * renal or hepatic dysfunction * ASA physical status \> 3
Study Locations (1)
University Hospital Center and University
Lausanne, Canton of Vaud, Switzerland