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Nitrous Oxide: 70% N2O (FiO2 0.3) vs N2O Free Group (FiO2 0.3): 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.

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

Measures 6

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

MeasureValue95% interval, lower95% interval, upperMethodNoteSource
Risk in group 10.08130.07260.0908wilsonClinicalTrials.gov
Risk in group 20.08440.07560.094wilsonClinicalTrials.gov
Risk difference, group 1 minus group 2-0.0031-0.0160.00984newcombe hybrid scoreClinicalTrials.gov
Risk ratio, group 1 over group 20.9630.8241.13logClinicalTrials.gov
Odds ratio, group 1 over group 20.960.811.14logClinicalTrials.gov
Number needed to treat, for one fewer participant with the outcome on Nitrous Oxide: 70% N2O (FiO2 0.3) than on N2O Free Group (FiO2 0.3)322from the risk difference intervalthe interval includes no differenceClinicalTrials.gov

Groups 2

Neither group, or both, names a comparator, so the groups keep ClinicalTrials.gov's order.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov codeSource
Group 1Nitrous Oxide: 70% N2O (FiO2 0.3)N2O Group (FiO2 0.3)~Nitrous Oxide: 70% N2O V's No N2O~Nitrous Oxide: N2O 70% v's No N2O2833,483OG000ClinicalTrials.gov
Group 2N2O Free Group (FiO2 0.3)N2O free group (FiO2 0.3)~Nitrous Oxide: 70% N2O V's No N2O~Nitrous Oxide: N2O 70% v's No N2O2963,509OG001ClinicalTrials.gov

Outcome 5

FieldValueSource
TypePRIMARYClinicalTrials.gov
TitleThe 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.ClinicalTrials.gov
DescriptionClinicalTrials.gov
Time frame30 days post opClinicalTrials.gov
PopulationClinicalTrials.gov

Trial 8

FieldValueSource
TitleThe ENIGMA II Trial:Nitrous Oxide Anaesthesia and Cardiac Morbidity After Major Surgery: a Randomised Controlled TrialClinicalTrials.gov
NCT numberNCT00430989ClinicalTrials.gov
PhasesPHASE4ClinicalTrials.gov
ConditionsCoronary Artery DiseaseClinicalTrials.gov
InterventionsNitrous Oxide, No Nitrous OxideClinicalTrials.gov
Lead sponsorBayside HealthClinicalTrials.gov
Results first posted2019-06-17ClinicalTrials.gov
Results on ClinicalTrials.govhttps://clinicaltrials.gov/study/NCT00430989?tab=resultsClinicalTrials.gov

Source 4

FieldValueSource
Releasetrial-comparisons-2026-03-23-0.1.0ClinicalTrials.gov
Release manifest SHA-256f66225897fbf258b57ea10bdacfd0347d3cdfda93f7f5685234b7e06ea36fa57ClinicalTrials.gov
AACT copy2026-03-23ClinicalTrials.gov
Tables readoutcome_counts.parquet, outcome_measurements.parquet, outcomes.parquet, reported_event_totals.parquet, reported_events.parquet, result_groups.parquet, studies.parquet, ctgov_trial.parquetClinicalTrials.gov

The same record as JSON

Release trial-comparisons-2026-03-23-0.1.0

ClinicalTrials.gov's posted results, through CTTI's AACT: ClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299 ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions. The measures are ConductScience's calculation from them.

ClinicalTrials.gov: none stated ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions. The measures are ConductScience's calculation from them.