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| Name | Class |
|---|---|
| National Institute of General Medical Sciences (NIGMS) | NIH |
| Foundation for Anesthesia Education and Research | OTHER |
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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.
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
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Treatment | Experimental | Vitamin B12 and folic acid |
|
| Comparator | Placebo Comparator | Nitrous oxide and placebo |
|
| Standard of care | Other | standard of care |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Vitamin B12 and folic acid | Drug | 1 mg vitamin B12 IV 5 mg folic acid IV in 100 ml NS infusion |
| |
| Measure | Description | Time Frame |
|---|---|---|
| Myocardial Ischemia | Measured by serial troponin and ECG | first 3 postoperative days |
| Measure | Description | Time Frame |
|---|---|---|
| Non-fatal MI | Myocardial Infarction per Third Definition of MI | 30 day postoperative |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Peter Nagele, MD | Washington University School of Medicine | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Barnes-Jewish Hospital | St Louis | Missouri | 63110 | United States |
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687 patients signed consent for enrollment; only 625 were analyzed.
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| ID | Title | Description |
|---|---|---|
| FG000 | 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 |
| FG001 | Comparator | Nitrous oxide and placebo Nitrous oxide and placebo |
| FG002 | Standard of Care | standard of care standard of care |
| Title | Milestones | Reasons Not Completed | ||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Overall Study |
|
|
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| ID | Title | Description |
|---|---|---|
| BG000 | 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 |
| BG001 | Comparator | Nitrous oxide and placebo Nitrous oxide and placebo |
| Units | Counts |
|---|---|
| Participants |
|
| Title | Description | Population Description | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Denominator Units Selected | Denominators | Classes |
|---|---|---|---|---|---|---|---|---|---|
| Age, Continuous | Mean |
| Type | Title | Description | Population Description | Reporting Status | Anticipated Posting Date | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Time Frame | Units Analyzed | Denominator Units Selected | Arm/Group Information | Denominators | Classes | Analyses | |||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Primary | Myocardial Ischemia | Measured by serial troponin and ECG | Posted | Count of Participants | Participants | first 3 postoperative days |
|
30 day
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| ID | Title | Description | Deaths (Affected) | Deaths (At Risk) | Serious Events (Affected) | Serious Events (At Risk) | Other Events (Affected) | Other Events (At Risk) |
|---|---|---|---|---|---|---|---|---|
| EG000 | 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 |
| Term | Organ System | Source Vocabulary | Assessment Type | Notes | Statistical Information |
|---|---|---|---|---|---|
| Death | Cardiac disorders | Systematic Assessment |
| Term | Organ System | Source Vocabulary | Assessment Type | Notes | Statistical Information |
|---|---|---|---|---|---|
| Readmission | General disorders | Systematic Assessment |
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| Title | Organization | Phone | Extension | |
|---|---|---|---|---|
| Principal Investigator | University of Chicago Medicine | 7737022544 |
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| ID | Term |
|---|---|
| D003324 | Coronary Artery Disease |
| ID | Term |
|---|---|
| D003327 | Coronary Disease |
| D017202 | Myocardial Ischemia |
| D006331 | Heart Diseases |
| D002318 | Cardiovascular Diseases |
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| ID | Term |
|---|---|
| D014805 | Vitamin B 12 |
| D005492 | Folic Acid |
| D009609 | Nitrous Oxide |
| D059039 | Standard of Care |
| ID | Term |
|---|---|
| D045728 | Corrinoids |
| D045725 | Tetrapyrroles |
| D011758 | Pyrroles |
| D001393 | Azoles |
| D006573 |
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| Nitrous oxide and placebo |
| Drug |
|
| standard of care | Other |
|
| BG002 | Standard of Care | standard of care standard of care |
| BG003 | Total | Total of all reporting groups |
| years |
|
| Sex: Female, Male | Count of Participants | Participants |
|
| Region of Enrollment | Count of Participants | Participants |
|
| Smoking history | Count of Participants | Participants |
|
| Diabetes | Count of Participants | Participants |
|
| Hypertension | Count of Participants | Participants |
|
| Chronic renal failute | Count of Participants | Participants |
|
| on hemodialysis | Count of Participants | Participants |
|
| Coronary artery disease | Count of Participants | Participants |
|
| Congestive heart failure | Count of Participants | Participants |
|
| Peripheral vascular disease | Count of Participants | Participants |
|
| ASA staging | ASA (American Society of Anesthesiologists) Physical status classification: ASA 1 = Normal healthy patient ASA 2 = Patient w/ mild systemic disease ASA 3 = Patient w/ severe systemic disease ASA 4 = Patient w/ severe systemic disease that is a constant threat to life ASA 5 = Moribund patient who's not expected to survive without the operation ASA 6 = Declared brain-dead patient, organs are being removed for donor purposes Higher values reflect worse disease status. | Count of Participants | Participants |
|
| Lee's revised cardiac risk index (Mean | Lee's Revised Cardiac Risk Index Rapid pre-op assessment using the Revised Cardiac Risk Index Patients receive 1 point for meeting a criteria; then totaled to get their prospective risk level. High risk surgery Having Coronary Artery Disease Having Congestive Heart Failure Having Cerebrovascular Disease Having Diabetes Mellitus and on insulin Having a Serum Creatinine >2 mg/dl or >177 μmol/L Higher totals connote higher risk (range 0-6) | Mean | Standard Deviation | units on a scale |
|
| Plasma total homocysteine mol/L | Mean | Standard Deviation | mcmol/L |
|
| MTHFR C677T polymorphism | The MTHFR C677T polymorphism reduces MTHFR enzyme activity; therefore, these patients have higher risk factors for coronary artery disease, acute myocardial infarction, peripheral vascular artery disease, stroke, or venous thromboembolism; having increased basal homocysteine levels or an abnormal methionine-load test (e.g., deficiency of vitamins B12, B6, and folic acid). | Some patients had missing genotype | Count of Participants | Participants |
|
| MTHFR A1298C plymorphism | The MTHFR A1298C polymorphism reduces MTHFR enzyme activity; therefore, these patients have higher risk factors for coronary artery disease, acute myocardial infarction, peripheral vascular artery disease, stroke, or venous thromboembolism; having increased basal homocysteine levels or an abnormal methionine-load test (e.g., deficiency of vitamins B12, B6, and folic acid). | Some patients had missing genotypes | Count of Participants | Participants |
|
| Medications Aspirin | Count of Participants | Participants |
|
| Medications Clopidogrel | Count of Participants | Participants |
|
| Medications Warfarin | Count of Participants | Participants |
|
| Medications Beta-Blocker | Count of Participants | Participants |
|
| ACE-Inhibitor | Count of Participants | Participants |
|
| Statin | Count of Participants | Participants |
|
| Diuretic | Count of Participants | Participants |
|
| Surgical procedure Vascular | Count of Participants | Participants |
|
| Surgical procedure Orthopedic | Count of Participants | Participants |
|
| Surgical procedure ENT | Count of Participants | Participants |
|
| Surgical procedure gyn | Count of Participants | Participants |
|
| Surgical procedure Urology | Count of Participants | Participants |
|
|
|
| Secondary | Non-fatal MI | Myocardial Infarction per Third Definition of MI | Posted | Count of Participants | Participants | 30 day postoperative |
|
|
|
| 0 |
| 250 |
| 0 |
| 250 |
| 39 |
| 250 |
| EG001 | Comparator | Nitrous oxide and placebo Nitrous oxide and placebo | 3 | 250 | 3 | 250 | 61 | 250 |
| EG002 | Standard of Care | standard of care standard of care | 1 | 125 | 1 | 125 | 27 | 125 |
| Wound Infection | Infections and infestations | Systematic Assessment |
|
| Any Pulmonary | Respiratory, thoracic and mediastinal disorders | Systematic Assessment |
|
| Cardiovascular | Cardiac disorders | Systematic Assessment |
|
| Renal | Renal and urinary disorders | Systematic Assessment |
|
| Bleeding | Blood and lymphatic system disorders | Systematic Assessment |
|
| Ileus | Gastrointestinal disorders | Systematic Assessment |
|
| Deep venous thrombosis | Vascular disorders | Systematic Assessment |
|
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| D001161 |
| Arteriosclerosis |
| D001157 | Arterial Occlusive Diseases |
| D014652 | Vascular Diseases |
| Heterocyclic Compounds, 1-Ring |
| D006571 | Heterocyclic Compounds |
| D006576 | Heterocyclic Compounds, 4 or More Rings |
| D000072471 | Heterocyclic Compounds, Fused-Ring |
| D047028 | Macrocyclic Compounds |
| D011083 | Polycyclic Compounds |
| D011622 | Pterins |
| D011621 | Pteridines |
| D006574 | Heterocyclic Compounds, 2-Ring |
| D009589 | Nitrogen Oxides |
| D005740 | Gases |
| D007287 | Inorganic Chemicals |
| D017672 | Nitrogen Compounds |
| D010087 | Oxides |
| D017601 | Oxygen Compounds |
| D019984 | Quality Indicators, Health Care |
| D011787 | Quality of Health Care |
| D006298 | Health Services Administration |
| D017530 | Health Care Quality, Access, and Evaluation |
| Male |
|
|
|
|
| 677CT |
|
| 677TT |
|
| 1298AC |
|
| 1298CC |
|