Clinical Trials Directory

Trials / Terminated

TerminatedNCT00802048

Local Anesthetic Infusion and Sternotomy

Study of Effectiveness of a Ropivacaïne Continuous Sternal Infusion to Reduce Postoperative Hyperalgesia Induced by Sternotomy After Cardiac Surgery

Status
Terminated
Phase
Phase 3
Study type
Interventional
Enrollment
21 (actual)
Sponsor
University Hospital, Bordeaux · Academic / Other
Sex
All
Age
50 Years – 75 Years
Healthy volunteers
Not accepted

Summary

Cardiac surgery often induces acute postoperative pain and moreover chronic dysesthesia frequently occur long-term after sternotomy. The high doses of intraoperative opioïds are well known to enhance postoperative hyperalgesia (HA) and a perioperative local anesthetic agent infusion is one of the therapeutic strategies used to limit this phenomena. The aim of this study was to evaluate the effectiveness of a continuous Ropivacaïne sternal infusion compared with a saline serum infusion to limit postoperative HA, pain and morphine consumption (M) after sternotomy in cardiac surgery. This strategy could lead to lower postoperative morphine consumption and opioïd induced hyperalgesia.

Detailed description

* Principal Objective: comparison of peri-incisionnal dynamic hyperalgesia extend evaluated by Von Frey filament during the first postoperative week between the two groups. * Secondary Objective: comparison of peri-incisionnal static hyperalgesia (pain threshold) extend evaluated by Von Frey filament, postoperative pain scores, morphine consumption, hemodynamic and respiratory parameters during the first postoperative week and incidence of chronic pain and dysesthesia at six month between the two groups. Ropivacaïne plasmatic concentration will be monitored, during infusion. * Study design : monocentric, double blind randomized clinical trial comparing two groups of patients with a same intraoperative anesthetic management : * Group 1: Ropivacaïne infiltration before skin incision followed by a 48 hours Ropivacaïne continuous infusion after surgery through a sternal fenestrated catheter * Group 2: same protocol with pre and postoperative saline infusion Postoperative pain management is identical in the two groups based upon a Morphine sulfate PCA pump for the first 48 hours. • Number of subjects : 40 patients, 20 in each group

Conditions

Interventions

TypeNameDescription
DRUGLocal anesthetic (Ropivacaine)Local anesthetic infusion
DRUGSalineSaline serum infusion

Timeline

Start date
2009-02-01
Primary completion
2010-01-01
Completion
2010-08-01
First posted
2008-12-04
Last updated
2011-12-13

Locations

1 site across 1 country: France

Source: ClinicalTrials.gov record NCT00802048. Inclusion in this directory is not an endorsement.