Multimodal anesthesia for beating heart surgery
Phase 2
- Conditions
- Coronary artery disease
- Registration Number
- RPCEC00000131
- Lead Sponsor
- Surgical-Clinic Hermanos Ameijeiras Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 90
Inclusion Criteria
1.Without previous cardiac surgery. 2.Ejection fraction >45 % without need of intra-aortic balloon pump support. 3.Without dysrhythmias. 4.Consciousness-awake and alert and without neurologic deficiency. 5.Urine output >0.5ml/kg and creatinine under 132 mmol/l. 6.Normal chest x-ray findings.
Exclusion Criteria
1.No consent. 2.Absolute contraindication of regional anesthesia. 3.Acute (less than 7 days of evolutions) or recent (less than 30 days) myocardial infarction. 4.Used of inotropic drug. 5.Sings of heart failure. 6.Middle or severe Lung Hypertension. 7.Chronic obstructive lung disease.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Postoperative analgesia (Pain intensity using a Visual Analog Scale). Measurement time: 1 hour (h), 2h , 3h, 4h, 12h, 24h, 48h and 72h after the extubation of the patient. Total doses of morphine used in the postoperative period (mg).Measurement time: At leave to the postoperative intensive care unit. Time to extubation (Hours between the end of the surgery and the extubation of the patient).
- Secondary Outcome Measures
Name Time Method