Ignite Creation Date:
2024-05-05 @ 6:33 PM
Last Modification Date:
2024-10-26 @ 9:35 AM
Study NCT ID:
NCT00508300
Status:
COMPLETED
Last Update Posted:
2020-08-11
First Post:
2007-07-26
Brief Title:
Epidural Analgesia EDA Versus Patient Controlled Analgesia PCA in Laparoscopic Colon Surgery
Sponsor:
University of Lausanne Hospitals
Organization:
University of Lausanne Hospitals
Study Overview
Official Title:
Epidural Analgesia EDA Versus Patient Controlled Analgesia PCA in Laparoscopic Colon Surgery A Monocentric Controlled Non-blinded Randomized Superiority Trial
Status:
COMPLETED
Status Verified Date:
2020-07
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
EVA
Brief 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
Detailed 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 01 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
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 01 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 Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None