Status:
COMPLETED
Functional Restoration After Abdominal and Pelvic Laparoscopic Surgery: Effect of Perioperative Intravenous Lidocaine
Lead Sponsor:
McGill University Health Centre/Research Institute of the McGill University Health Centre
Conditions:
Colon Cancer
Inflammatory Bowel Diseases
Eligibility:
All Genders
18-85 years
Phase:
NA
Brief Summary
This is a blinded randomized controlled trial in patients undergoing laparoscopic colon surgery. The aim of this study is to assess whether perioperative intravenous lidocaine has an impact on the ear...
Detailed Description
This is a blinded randomised study of patients undergoing major laparoscopic abdominal and pelvic surgery. The first group of patients will receive thoracic epidural analgesia, the second group will r...
Eligibility Criteria
Inclusion
- patients scheduled to undergo laparoscopic colonic resection
Exclusion
- patients who have trouble to understand, read or communicate either in French or in English
- dementia
- patients suffering from severe physical disability (arthritis, neuromuscular dysfunction, stroke, paraplegia) or inability to walk or conduct daily activity
- patients suffering from severe cardiac or respiratory disease (status ASA IV)
- patients suffering from metastatic carcinoma
- patients who have a history of chemoradiation within the six months preceding surgery
- allergy to lidocaine
- morbid obesity
Key Trial Info
Start Date :
July 1 2009
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
June 1 2011
Estimated Enrollment :
60 Patients enrolled
Trial Details
Trial ID
NCT00982618
Start Date
July 1 2009
End Date
June 1 2011
Last Update
November 28 2011
Active Locations (1)
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1
Montreal General Hospital
Montreal, Quebec, Canada, H3G 1A4