Viewing Study NCT01196767



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Last Modification Date: 2024-10-26 @ 10:24 AM
Study NCT ID: NCT01196767
Status: COMPLETED
Last Update Posted: 2013-04-04
First Post: 2010-07-26

Brief Title: Ropivacaine Though Laterosternal Catheters After Cardiac Surgery
Sponsor: University Hospital Clermont-Ferrand
Organization: University Hospital Clermont-Ferrand

Study Overview

Official Title: Postoperative Analgesia After Cardiac Surgery Effects of a Continuous Infusion of Ropivacaine Through Laterosternal Catheters
Status: COMPLETED
Status Verified Date: 2013-04
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: None
Brief Summary: This is a prospective double-blinded and randomised study involving patients undergoing cardiac surgery with median sternotomy the effects on postoperative analgesia of a 48-hr continuous infusion of ropivacaine 2 mgmL-1 at the rate of 4 mLhr-1 through two catheters inserted at the lateral edges of the sternum will be studied versus a control group in which normal saline will be infused in the same conditions
Detailed Description: Diverse methods for infusion of local anaesthetics after cardiac surgery have been proposed but none of them provided high-level evidence of efficacy The catheters studied here are designed for a surgical insertion before closure of the sternotomy with the aim of infusing the drug the closest possible of the terminations of intercostal nerves

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