Kuopio University hospital
Kuopio, FI70029, Finland
NCT Number: NCT02449486
Continuous ropivacaine infusion to sternotomy wound after coronary artery bypass grafting (CABG) or heart valve surgery to diminish postoperative pain.
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Notify Me18 year–80 year
All sexes
Interventional
Phase 4
Kuopio, FI70029, Finland
A multiporous catheter will be introduced into sternotomy wound to CABG or heart valve surgery patients and continuous ropivacaine infusion 4 ml/h will be started immediately after surgery. Ropivacaine infusion will be administered during 48 postoperative hours. All patients receive patient controlled analgesia (PCA) oxycodone after extubation in the PACU. All patients receive a standardized anesthesia during surgery.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Time frame: 48 postoperative hours
postoperative PCA administered oxycodone
Time frame: 48 postoperative hours
pain measured with VAS at rest and on movement
Kuopio University Hospital
Other
Ropivacaine Infusion to Alleviate Postoperative Pain After Cardiac Surgery
Acronym: NAROSYD
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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