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Clinical Trials/NCT01601795
NCT01601795
Completed
Phase 4

Sevoflurane and Isoflurane - Cardioprotective Effects, Hemodynamic Stability and Pharmacokinetics During Cardiopulmonary Bypass With the MECC System

University Hospital, Basel, Switzerland1 site in 1 country30 target enrollmentJuly 2012

Overview

Phase
Phase 4
Intervention
Sevoflurane
Conditions
Myocardial Reperfusion Injury
Sponsor
University Hospital, Basel, Switzerland
Enrollment
30
Locations
1
Primary Endpoint
postoperative maximum Troponin levels
Status
Completed
Last Updated
12 years ago

Overview

Brief Summary

The use of volatile anesthetics in cardiac anesthesia is very common, because of their cardioprotective effects and their ability to ensure a sufficient depth of anesthesia. In line with the development of fast track concepts in cardiac anesthesia, volatile anesthetics are widely used to avoid a delayed recovery from cardiac surgery and anesthesia. Volatile anesthetics are delivered from calibrated vaporizers in the anesthesia machine or the cardiopulmonary bypass machine (during extracorporeal circulation).

Isoflurane and Sevoflurane are the most commonly used volatile anesthetics in patients undergoing cardiopulmonary bypass (CPB). The vaporizer of the anesthetics is on the cardiopulmonary bypass machine and the volatile agent is blended with air and oxygen. Until now, the pharmacokinetics of halothane, enflurane, isoflurane and desflurane during CPB have been described.

Sevoflurane might be of advantage because of additional myocardial protective effects during cardiac anesthesia and cardiopulmonary bypass. However, the pharmacokinetics of sevoflurane during CPB have not been investigated so far, although its being used at many hospitals.

The investigators will conduct a randomized prospective study with either sevoflurane or isoflurane during cardiopulmonary bypass surgery. The study will help to answer the questions about the possible cardioprotective effects of the widely used volatile anesthetics and the hemodynamic stability during cardiopulmonary bypass. Knowing the pharmacokinetics of these drugs allows the anesthesiologist to titrate the volatile anesthetics more precise.

The investigators hypothesizes that the maximal postoperative increase in troponin T will be smaller in the sevoflurane group than in the isoflurane group. The investigators hypothesizes that the total amount of noradrenaline needed during the entire period of cardiopulmonary bypass will be smaller in the sevoflurane group than in the isoflurane group. The investigators hypothesizes that kinetics of washin and washout at the CPB will be faster in the sevoflurane group than in the isoflurane group. The investigators hypothesizes that the time to extubation, respectively the length of stay in intensive care unit and hospital is shorter in the sevoflurane group than in the isoflurane group.

Detailed Description

Endpoints Primary Endpoint: Troponin The study will compare the maximum postoperative troponin levels in the isoflurane and sevoflurane groups as a direct quantitative marker of damaged myocardial cells. Maximum troponin levels should be reached within the first 24 hours after surgery. Secondary Endpoints: A) Hemodynamic stability during on-pump The investigators will compare the hemodynamic stability during CPB between the isoflurane and sevoflurane group. Therefore the total dosage of noradrenaline used during the surgery will be measured. B) Washin and Washout Kinetic Kinetics of washin and washout of sevoflurane and isoflurane during CPB will be investigated and described. C) Extubation time and length of stay in the intensive care and in hospital Time to extubation and the length of stay in intensive care unit and in hospital will be documented. D) Mortality after 30 days The mortality after 30 days will also be monitored. If the patient is no more in the hospital a phone call will be made.

Registry
clinicaltrials.gov
Start Date
July 2012
End Date
January 2014
Last Updated
12 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
University Hospital, Basel, Switzerland
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • elective coronary bypass surgery
  • preserved left ventricular function (LVEF (left ventricular ejection fraction) \>55%)
  • Age \> 18 years
  • planned MECC-System (minimized extracorporeal circulation)
  • informed consent

Exclusion Criteria

  • chronic renal insufficiency (serum creatinine \> 132umol/l)
  • Body Mass Index \> 35kg/m2
  • additional operative procedures (eg. valve replacement/reconstruction)
  • recent cardiac infarction (\< 7 days) or elevated cardiac enzymes the day before surgery
  • previous cardiac operation
  • Pregnancy / Lactation
  • known malignant hyperthermia (MH) or known relatives with MH
  • known allergy against propofol, history of propofol infusion syndrome
  • Drug abuse (cocaine, amphetamine, heroine, cannabis)
  • non-judicious persons

Arms & Interventions

Sevoflurane

During cardiopulmonary bypass, sevoflurane will be administered through a vaporizer integrated into heart-lung-machine.

Intervention: Sevoflurane

Isoflurane

During cardiopulmonary bypass, isoflurane will be administered through a vaporizer integrated into heart-lung-machine.

Intervention: Isoflurane

Outcomes

Primary Outcomes

postoperative maximum Troponin levels

Time Frame: 24 hours

Secondary Outcomes

  • Hemodynamic stability during on-pump(2 hours)

Study Sites (1)

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