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TEAM-Project: Trial on the Effect of Anesthetics on Morbidity and Mortality

University Hospital Basel logo

University Hospital Basel

Status and phase

Completed
Phase 4

Conditions

Coronary Artery Disease

Treatments

Drug: Intravenous anesthetic, propofol
Drug: Inhalational anesthetic

Study type

Interventional

Funder types

Other
Industry

Identifiers

NCT00286585
261/05
IIS-SWIT-05-002

Details and patient eligibility

About

Volatile anesthetics may provide some protection from myocardial ischemia, an effect called anesthetic preconditioning. In patients undergoing coronary artery bypass surgery, this preconditioning effect resulted in better cardiac performance, faster recovery and lower morbidity and mortality.

The investigators will perform a prospective randomized multi-center study to compare volatile with total intravenous anesthesia in patients at a high cardiac risk who undergo major non-cardiac surgery.

Full description

Basic research and animal studies have detected that volatile anesthetics provide some protection from myocardial ischemia, an effect called anesthetic preconditioning. Recent clinical studies have found that this preconditioning effect is of clinical relevance in patients undergoing coronary artery bypass surgery, resulting in better cardiac function and faster recovery after surgery, and in lower one-year morbidity. In patients undergoing non cardiac surgery, cardiac complications also are the major cause of perioperative morbidity and mortality. Myocardial ischemia frequently occurs during and immediately after non cardiac surgery in patients with coronary artery disease, and is a strong predictor of subsequent cardiac complications and death. Whether or not volatile anesthetics also provide clinically relevant protection from perioperative ischemia and subsequent cardiac complications in patients undergoing non cardiac surgery is unknown. Therefore, we will perform a prospective, randomized multi-center study to compare volatile with total intravenous anesthesia in patients at high cardiac risk who undergo major non cardiac surgery. We hypothesize that the use of a volatile anesthetic will reduce the incidence of perioperative ischaemia and myocardial injury, as indicated primarily by less ST-segment changes in the Holter ECG and, if there will be an effect, secondarily by lower incidences of elevated troponin T and NT-pro-BNP levels. And we hypothesize that the use of a volatile anesthetic will reduce the one-year incidence of cardiac complications and all cause mortality after surgery. The results of this study may apply to a huge percentage of surgical patients because coronary artery disease is the clinically most relevant co-morbidity, and its prevalence is expected to increase with the steadily increasing number of surgical patients aged 65 yr and older.

Enrollment

385 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients scheduled for a non-cardiac surgical procedure of high or intermediate cardiac risk are eligible if they have documented coronary artery disease (CAD) or are at high risk of CAD.

Exclusion criteria

  • Ongoing medication with sulfonylurea derivatives (unless stopped ≥ 2 days before surgery) or theophylline
  • Emergency surgery
  • Unstable angina pectoris
  • Preoperative hemodynamic instability
  • Severe hepatic disease
  • Renal insufficiency (creatinine clearance < 30 ml/min)
  • Severe chronic obstructive pulmonary disease (forced expiratory volume in 1 second [FEV1] < 1 litre)
  • Absence of written patient consent

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

385 participants in 2 patient groups

Inhalational anesthetic
Active Comparator group
Description:
Sevoflurane will be used as the main anesthetic in this arm, and no propofol will be administered
Treatment:
Drug: Inhalational anesthetic
Intravenous anesthetic, propofol
Active Comparator group
Description:
Propofol will be used as the main anesthetic in this arm, and no inhalational anesthetic will be administered
Treatment:
Drug: Intravenous anesthetic, propofol

Trial contacts and locations

3

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Data sourced from clinicaltrials.gov

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