Clinical Trials Logo

Clinical Trial Summary

To investigate the real value of a fast track protocol compared to a standard care protocol regarding postoperative complications and hospital stay in a multicentric setting in an intention to treat fashion.


Clinical Trial Description

Our fast track protocol contains the four major components perioperative fluid restriction, epidural analgesia, early oral feeding and enforced mobilisation ;


Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT00556790
Study type Interventional
Source University of Lausanne Hospitals
Contact
Status Terminated
Phase N/A
Start date November 2004
Completion date January 2007