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Vitamins in Nitrous Oxide Study

Pharmacogenetics of Adverse Outcomes After Nitrous Oxide Anesthesia

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00655980
Acronym
VINO
Enrollment
687
Registered
2008-04-10
Start date
2008-02-29
Completion date
2016-12-31
Last updated
2020-10-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Coronary Artery Disease, Major Surgery

Brief summary

In this study, we want to find out if laughing gas (nitrous oxide) leads to a higher rate of cardiac complications after surgery in patients with a specific genetic profile (mutations in the MTHFR gene) and if this risk can be prevented by giving patients vitamin B12 and folate during surgery.

Detailed description

Background and significance: Recent studies have shown that nitrous oxide (N2O) anesthesia may be associated with an increased risk of adverse cardiovascular outcomes. It is well-known that N2O inhibits vitamin B12-dependent enzymes and as a result increases plasma homocysteine concentrations. Homocysteine has been identified as risk factor for cardiovascular disease. Therefore elevations in homocysteine after N2O may be a causative factor in N2O toxicity. In a previous investigation, we found that patients who carry a homozygous mutation in the MTHFR gene develop higher homocysteine levels after N2O anesthesia than non-carriers. These patients might be at higher risk for adverse cardiac outcomes from N2O. Thus, there may be a pharmacogenetic mechanism to account for the adverse cardiac outcomes from N2O. Moreover, prevention of N2O-increased homocysteine concentrations in these high risk patients by perioperative vitamin B12 and folate supplementation might decrease the incidence of adverse cardiac outcomes. Hypothesis: Patients carrying a homozygous MTHFR 677C\>T or 1298 A\>C variant allele will have a higher incidence rate of postoperative myocardial ischemia after N2O anesthesia \[detected by serial TnI measurements\] due to elevated homocysteine levels than normal wild-type non-carriers, and that the incidence rate will be reduced if they receive perioperative vitamin B12/folate supplementation. Primary outcome: Myocardial ischemia in the first 72 hours after surgery (measured by serial troponin and ECGs). Secondary outcome: Composite endpoint of 30-day mortality and major cardiac morbidity (non-fatal MI) Design: Randomized controlled trial. 500 patients will receive N2O during surgery and will be randomized to receive B-vitamins or placebo. 125 patients will receive no N2O and no B-vitamins (control arm). Mendelian randomization of MTHFR genotype. Intervention: IV vitamin B12 (1 mg) and folate (5 mg) pre- and postoperatively Study setting: Barnes-Jewish-Hospital, St. Louis, MO Patients: Patients scheduled for major surgery with or at risk for coronary artery disease

Interventions

DRUGNitrous oxide and placebo
OTHERstandard of care

1 mg vitamin B12 IV 5 mg folic acid IV in 100 ml NS infusion

Sponsors

National Institute of General Medical Sciences (NIGMS)
CollaboratorNIH
Foundation for Anesthesia Education and Research
CollaboratorOTHER
Washington University School of Medicine
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
FACTORIAL
Primary purpose
DIAGNOSTIC
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Adult patients; age \>18 yrs, ASA III-IV * Previously diagnosed coronary artery disease or at risk for coronary artery disease * Scheduled for major surgery (\>2 hrs)

Exclusion criteria

* Patients not expected to live past 24 hours (ASA 5) * Patients with significant pulmonary disease requiring supplemental oxygen * Patients taking supplemental vitamin B12 or folate * Contraindication against N2O (pneumothorax, mechanical bowel obstruction, middle ear occlusion, laparoscopic surgery, raised intracranial pressure) * Hypersensitivity to cobalamins * Leber's disease (hereditary optic nerve atrophy) \[vitamin B12 interaction\] * Seizure disorder \[folate interference\]

Design outcomes

Primary

MeasureTime frameDescription
Myocardial Ischemiafirst 3 postoperative daysMeasured by serial troponin and ECG

Secondary

MeasureTime frameDescription
Non-fatal MI30 day postoperativeMyocardial Infarction per Third Definition of MI

Countries

United States

Participant flow

Recruitment details

687 patients signed consent for enrollment; only 625 were analyzed.

Participants by arm

ArmCount
Treatment
Vitamin B12 and folic acid Vitamin B12 and folic acid: 1 mg vitamin B12 IV 5 mg folic acid IV in 100 ml NS infusion
250
Comparator
Nitrous oxide and placebo Nitrous oxide and placebo
250
Standard of Care
standard of care standard of care
125
Total625

Withdrawals & dropouts

PeriodReasonFG000FG001FG002
Overall Studysurgery canceled; or subject or anesthes26315

Baseline characteristics

CharacteristicTotalTreatmentComparatorStandard of Care
ACE-Inhibitor225 Participants94 Participants88 Participants43 Participants
Age, Continuous65.5 years
STANDARD_DEVIATION 10.7
64.7 years
STANDARD_DEVIATION 10.6
65.2 years
STANDARD_DEVIATION 10.7
67.6 years
STANDARD_DEVIATION 10.9
ASA staging
ASA 1-A normal healthy patient
1 Participants1 Participants0 Participants0 Participants
ASA staging
ASA 2 A patient with mild systemic disease
98 Participants45 Participants42 Participants11 Participants
ASA staging
ASA 3 - A patient with severe systemic disease
501 Participants199 Participants196 Participants106 Participants
ASA staging
ASA 4 -A patient with severe systemic disease tha
23 Participants5 Participants10 Participants8 Participants
Chronic renal failute67 Participants16 Participants35 Participants16 Participants
Congestive heart failure73 Participants27 Participants31 Participants15 Participants
Coronary artery disease372 Participants140 Participants148 Participants84 Participants
Diabetes223 Participants96 Participants88 Participants39 Participants
Diuretic194 Participants79 Participants87 Participants28 Participants
Hypertension504 Participants200 Participants204 Participants100 Participants
Lee's revised cardiac risk index (Mean2.0 units on a scale
STANDARD_DEVIATION 0.8
1.9 units on a scale
STANDARD_DEVIATION 0.8
2.0 units on a scale
STANDARD_DEVIATION 0.9
2.1 units on a scale
STANDARD_DEVIATION 0.8
Medications Aspirin332 Participants126 Participants137 Participants69 Participants
Medications Beta-Blocker330 Participants119 Participants141 Participants70 Participants
Medications Clopidogrel111 Participants42 Participants45 Participants24 Participants
Medications Warfarin62 Participants28 Participants21 Participants13 Participants
MTHFR A1298C plymorphism
1298AA
303 Participants133 Participants120 Participants50 Participants
MTHFR A1298C plymorphism
1298AC
236 Participants86 Participants105 Participants45 Participants
MTHFR A1298C plymorphism
1298CC
50 Participants24 Participants19 Participants7 Participants
MTHFR C677T polymorphism
677CC
324 Participants137 Participants130 Participants57 Participants
MTHFR C677T polymorphism
677CT
202 Participants76 Participants89 Participants37 Participants
MTHFR C677T polymorphism
677TT
63 Participants29 Participants26 Participants8 Participants
on hemodialysis5 Participants1 Participants3 Participants1 Participants
Peripheral vascular disease210 Participants81 Participants85 Participants44 Participants
Plasma total homocysteine mol/L13.1 mcmol/L
STANDARD_DEVIATION 5.5
13.5 mcmol/L
STANDARD_DEVIATION 5.7
13.4 mcmol/L
STANDARD_DEVIATION 5.8
11.6 mcmol/L
STANDARD_DEVIATION 4.2
Region of Enrollment
United States
625 Participants250 Participants250 Participants125 Participants
Sex: Female, Male
Female
234 Participants92 Participants97 Participants45 Participants
Sex: Female, Male
Male
391 Participants158 Participants153 Participants80 Participants
Smoking history464 Participants195 Participants175 Participants94 Participants
Statin345 Participants130 Participants146 Participants69 Participants
Surgical procedure ENT59 Participants22 Participants20 Participants17 Participants
Surgical procedure gyn55 Participants26 Participants21 Participants8 Participants
Surgical procedure Orthopedic194 Participants88 Participants81 Participants25 Participants
Surgical procedure Urology50 Participants22 Participants22 Participants6 Participants
Surgical procedure Vascular216 Participants76 Participants87 Participants53 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
EG002
affected / at risk
deaths
Total, all-cause mortality
0 / 2503 / 2501 / 125
other
Total, other adverse events
39 / 25061 / 25027 / 125
serious
Total, serious adverse events
0 / 2503 / 2501 / 125

Outcome results

Primary

Myocardial Ischemia

Measured by serial troponin and ECG

Time frame: first 3 postoperative days

ArmMeasureCategoryValue (COUNT_OF_PARTICIPANTS)
B-Vitamin GroupMyocardial IschemiaCardiac troponin elevation33 Participants
B-Vitamin GroupMyocardial IschemiaNo Cardiac troponin elevation217 Participants
ComparatorMyocardial IschemiaCardiac troponin elevation34 Participants
ComparatorMyocardial IschemiaNo Cardiac troponin elevation216 Participants
Standard of CareMyocardial IschemiaCardiac troponin elevation17 Participants
Standard of CareMyocardial IschemiaNo Cardiac troponin elevation108 Participants
Secondary

Non-fatal MI

Myocardial Infarction per Third Definition of MI

Time frame: 30 day postoperative

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
B-Vitamin GroupNon-fatal MI7 Participants
ComparatorNon-fatal MI15 Participants
Standard of CareNon-fatal MI8 Participants

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026