Reduce Nonsteroidal Antiinflammatory Drugs Doses for Analgesia After Sternotomy (LoDoNSAID)
Cardiac Surgery, Post-operative Pain
About this trial
This is an interventional treatment trial for Cardiac Surgery focused on measuring Cardiac surgery, Post-operative pain, Kétoprofène, Minimum analgesic dose, Morphin consumption, Morphin secondary effects, Patient comfort and satisfaction, Renal fonction
Eligibility Criteria
Inclusion Criteria:
- Patients scheduled for a cardiac surgery (Coronary artery bypass graft, valve replacement)
- Age over 18 years
- Weight between 60 and 100 kg
- Absence of criteria for non-inclusion
Exclusion Criteria:
- Age over 75 years
- Renal insufficiency (MDRD <60 ml / min)
- Hepatic Insufficiency
- Congestive heart failure (EF <40%)
- Insulin-requiring diabetes
- Preoperative coagulation trouble
- History of peptic ulcer or gastrointestinal bleeding
- Allergy to NSAIDs
- Surgery in emergency, aorta surgery, heart transplantation
- Peptic ulcer scalable, history of peptic ulcer or recurrent bleeding (2 or more distinct episodes of bleeding or ulceration objectified)
- Pregnant or lactating women
- Major protected
Sites / Locations
- CHU de Clermont-FerrandRecruiting
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
Placebo Comparator
Other
Other
Other
placebo group
ketopofen quarter dose
ketoprofen half-dose
Ketoprofen full dose
Group 1 : Placebo group (P). 0 mg/kg ketoprofen IV every 6 hours for 48 hours (or 0 mg/kg every 24 hours) for 48 hours
Group 2 : "Ketoprofen quarter dose" (K ¼). 0,125 mg/kg ketoprofen IV every 6 hours (0,5 mg/kg every 24 hours) for 48 hours.
Group 3 : "Ketoprofen half-dose" (K ½). 0,25 mg/kg ketoprofen IV every 6 hours (1 mg/kg every 24 hours) for 48 hours.
Group 4 : "Ketoprofen full dose" (KPD). 0,5 mg/kg ketoprofen IV every 6 hours (or 2 mg/kg every 24 hours) for 48 hours