Skip to main content
OpenTrials
Completed

NCT Number: NCT00430989

The ENIGMA II Trial:Nitrous Oxide Anaesthesia and Cardiac Morbidity After Major Surgery: a Randomised Controlled Trial

To investigate the safety of nitrous oxide (N2O) anaesthesia in patients with risk factors for coronary artery disease undergoing major surgery.

Completed

Looking for future studies?

Notify Me

Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

Alfred Hosptial

Melbourne, Victoria, 3004, Australia

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Adult males and females age ≥ 45 years, undergoing noncardiac surgery and general anaesthesia expected to exceed two hours.
  • At increased risk of cardiac events, defined as any of
  • history of coronary artery disease as defined by a history of any one of the following: i. angina ii. MI iii. segmental wall motion abnormality on echocardiography or a fixed defect on radionuclide imaging iv. a positive exercise stress test for cardiac ischaemia v. a positive radionuclide exercise, echocardiographic exercise, or pharmacological cardiovascular stress test for cardiac ischaemia vi. coronary revascularization (CABG or PTCA) vii. angiographic evidence of atherosclerotic stenosis > 50% of the diameter of any coronary artery viii. ECG with pathological Q waves in two contiguous leads
  • heart failure
  • cerebrovascular disease thought due to atherothrombotic disease
  • aortic or peripheral vascular disease
  • or three or more of the following risk factors:
  • age ≥70 years
  • any history of congestive heart failure
  • diabetes and currently on an oral hypoglycaemic agent or insulin therapy
  • current treatment for hypertension
  • preoperative serum creatinine >175 micro mol/L (> 2.0 mg/dl)
  • current or previous high cholesterol ≥6.2 mmol/L (> 240 mg/dl)
  • history of a transient ischemic attack (TIA) (i.e. a transient focal neurological deficit that lasted less than 24 hours and thought to be vascular in origin)
  • emergency/urgent surgery (i.e. surgery which must be undertaken within 24 hours of acute presentation to hospital)
  • high-risk type of surgery (i.e. intrathoracic or intraperitoneal)

Exclusion criteria

  • having cardiac surgery
  • marked impairment of gas-exchange expected to require Fi02> 0.5 intraoperatively
  • specific circumstances where N2O is contraindicated (eg. volvulus, pulmonary hypertension, raised intracranial pressure) or the anaesthetist plans to use supplemental oxygen (eg. colorectal surgery)
  • N2O unavailable for use.

Treatment and study plan

Nitrous Oxide

Other

General anaesthesia with the inclusion of Nitrous Oxide at 70%

No Nitrous Oxide

Other

General anaesthesia with no use of Nitrous Oxide

Primary outcomes

  1. The Primary Endpoint is a Composite of Death and Cardiovascular Events (Clinical and Silent MI, Cardiac Failure, Cardiac Arrest, Pulmonary Embolism, and Stroke) Measured at 30 Days After Surgery.

    Time frame: 30 days post op

Secondary outcomes

  1. Myocardial Infarction (MI)

    Time frame: 30 days post op

  2. Cardiac Arrest

    Time frame: 30 days

  3. Pulmonary Embolism

    Time frame: 30 Days Post op

  4. Stroke

    Time frame: 30 Days Post op

  5. Wound Infection

    Time frame: 30 Days Post op

  6. Hospital Stay (Days)

    Time frame: 30 Days Post Op

Sponsors and collaborators

Lead sponsor

Bayside Health

Other Gov

Collaborators

  • National Health and Medical Research Council, Australia

Registry information

Official study title

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]).

Important dates

Study start
2007
Primary completion
2013
Study completion
2013
First posted
Feb 2, 2007
Registry last updated
Jan 20, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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.

Published trials that share one or more normalized conditions with this study.