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Clinical Trial Summary

The purpose of this study is to determine whether a epidural analgesia versus patient controlled analgesia reduces the medical recovery in patients undergoing elective laparoscopic colon surgery.


Clinical Trial Description

Allocation by individual random number generated by a computer program to either EDA or PCA for 48h after laparoscopic colonic surgery.

Short, both groups are treated according to a recent Fast track protocol. Group A will preoperatively receive a mid thoracic EDA (th 8-9; naropine 0,1%) while group B will receive a PCA (morphine) postoperatively. Both EDA and PCA are removed the afternoon at day 2. Patients with a non-functioning EDA within the first 24h will be crossed over to the PCA group. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT00508300
Study type Interventional
Source University of Lausanne Hospitals
Contact
Status Completed
Phase N/A
Start date January 2010
Completion date October 2013

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