Vitamins in Nitrous Oxide Study (VINO)
Primary Purpose
Major Surgery, Coronary Artery Disease
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Vitamin B12 and folic acid
Nitrous oxide and placebo
standard of care
Sponsored by

About this trial
This is an interventional diagnostic trial for Major Surgery
Eligibility Criteria
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]
Sites / Locations
- Barnes-Jewish Hospital
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Experimental
Placebo Comparator
Other
Arm Label
Treatment
Comparator
Standard of care
Arm Description
Vitamin B12 and folic acid
Nitrous oxide and placebo
standard of care
Outcomes
Primary Outcome Measures
Myocardial Ischemia
Measured by serial troponin and ECG
Secondary Outcome Measures
Non-fatal MI
Myocardial Infarction per Third Definition of MI
Full Information
NCT ID
NCT00655980
First Posted
April 4, 2008
Last Updated
September 8, 2020
Sponsor
Washington University School of Medicine
Collaborators
National Institute of General Medical Sciences (NIGMS), Foundation for Anesthesia Education and Research
1. Study Identification
Unique Protocol Identification Number
NCT00655980
Brief Title
Vitamins in Nitrous Oxide Study
Acronym
VINO
Official Title
Pharmacogenetics of Adverse Outcomes After Nitrous Oxide Anesthesia
Study Type
Interventional
2. Study Status
Record Verification Date
September 2020
Overall Recruitment Status
Completed
Study Start Date
February 2008 (undefined)
Primary Completion Date
December 2016 (Actual)
Study Completion Date
December 2016 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Washington University School of Medicine
Collaborators
National Institute of General Medical Sciences (NIGMS), Foundation for Anesthesia Education and Research
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
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
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Major Surgery, Coronary Artery Disease
7. Study Design
Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Factorial Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
687 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Treatment
Arm Type
Experimental
Arm Description
Vitamin B12 and folic acid
Arm Title
Comparator
Arm Type
Placebo Comparator
Arm Description
Nitrous oxide and placebo
Arm Title
Standard of care
Arm Type
Other
Arm Description
standard of care
Intervention Type
Drug
Intervention Name(s)
Vitamin B12 and folic acid
Intervention Description
1 mg vitamin B12 IV 5 mg folic acid IV in 100 ml NS infusion
Intervention Type
Drug
Intervention Name(s)
Nitrous oxide and placebo
Intervention Type
Other
Intervention Name(s)
standard of care
Primary Outcome Measure Information:
Title
Myocardial Ischemia
Description
Measured by serial troponin and ECG
Time Frame
first 3 postoperative days
Secondary Outcome Measure Information:
Title
Non-fatal MI
Description
Myocardial Infarction per Third Definition of MI
Time Frame
30 day postoperative
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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]
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Peter Nagele, MD
Organizational Affiliation
Washington University School of Medicine
Official's Role
Principal Investigator
Facility Information:
Facility Name
Barnes-Jewish Hospital
City
Saint Louis
State/Province
Missouri
ZIP/Postal Code
63110
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Vitamins in Nitrous Oxide Study
We'll reach out to this number within 24 hrs