Alfred Hosptial
Melbourne, Victoria, 3004, Australia
NCT Number: NCT00430989
To investigate the safety of nitrous oxide (N2O) anaesthesia in patients with risk factors for coronary artery disease undergoing major surgery.
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Notify Me18 year and older
All sexes
Interventional
Phase 4
Melbourne, Victoria, 3004, Australia
Approximately 25% of patients undergoing major surgery have known coronary artery disease (CAD) or risk factors for CAD.
N2O interferes with vitamin B12 and folate metabolism. This impairs production of methionine (from homocysteine), used to form tetrahydrofolate and thymidine during DNA synthesis. It has been repeatedly demonstrated that N2O anaesthesia increases postoperative homocysteine levels. Chronic hyperhomocysteinaemia is associated with cardiovascular disease, and acute hyperhomocysteinaemia is known to cause endothelial dysfunction. One small trial has demonstrated an increased incidence of postoperative myocardial ischaemia in patients receiving N2O anaesthesia. Reducing postoperative myocardial infarction and death are important aims for those with CAD undergoing major surgery.
Our previous trial (ENIGMA) studied 2050 patients and identified some serious adverse effects, but most patients were not at risk of CAD and so we could not reliably assess serious cardiac complications. We propose a large simple randomized clinical trial of 7,000 patients to provide a definitive evaluation of the safety of N2O anaesthesia.
Updated statistical analysis plan can be found at www.enigma2.org.au.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
General anaesthesia with the inclusion of Nitrous Oxide at 70%
General anaesthesia with no use of Nitrous Oxide
Time frame: 30 days post op
Time frame: 30 days post op
Time frame: 30 days
Time frame: 30 Days Post op
Time frame: 30 Days Post op
Time frame: 30 Days Post op
Time frame: 30 Days Post Op
Bayside Health
Other Gov
Large, Randomised, Parallel-group, Controlled Trial, With Patients Randomly Allocated to Either N2O-containing (70% N2O in Oxygen [FiO2 0.3]) or N2O-free (70% Nitrogen in Oxygen [FiO2 0.3]).
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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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