WENBIT - Western Norway B Vitamin Intervention Trial

This study has been completed.
Sponsor:
Collaborators:
The Research Council of Norway
Norwegian Foundation for Health and Rehabilitation
Norwegian Heart and Lung Patient Organisation
The Royal Norwegian Ministry of Health
Locus for Homocysteine and Related Vitamins, University of Bergen, Norway
Locus for Cardiac Research, University of Bergen, Norway
Foundation to Promote Research into Functional Vitamin B12 Deficiency, Bergen, Norway
Alpharma Pharmaceuticals LLC, a subsidiary of Pfizer Inc.
Information provided by (Responsible Party):
Haukeland University Hospital
ClinicalTrials.gov Identifier:
NCT00354081
First received: July 19, 2006
Last updated: July 11, 2013
Last verified: May 2010
  Purpose

PURPOSE OF STUDY Observational studies have demonstrated that elevated levels of plasma total homocysteine is a risk factor for cardiovascular disease. The purpose of this trial is to evaluate the clinical effects of homocysteine lowering treatment with B vitamins during 3-5 years follow-up of patients undergoing cardiac catheterization for suspected coronary artery disease (CAD). Special attention will be given to complication rates among patients needing subsequent percutaneous transluminal coronary angioplasty (PCI) or coronary artery by-pass grafting (CABG).

HYPOTHESIS The primary hypothesis of this study is that, among patients with CAD, a daily supplement with B vitamins will reduce the risk for cardiovascular mortality and serious cardiovascular events with at least 20%. The secondary hypothesis of this study is that, among patients with CAD, a daily supplement with B vitamins will reduce the risk for total mortality, coronary events, cerebrovascular events and other cardiovascular events. The hypothesis will be tested for an effect of any of the treatments (folic acid / vitamin B12 or B6), and the effect will be evaluated according to initial total homocysteine levels and B vitamin levels as well as to the change in these levels after 1 and 6 months. The sample size has been calculated to 3088 patients using a two-sided chi-square test with significance 0.05 and at an 80% power level, presumed event rate of 22% over 4 years, and event rate reduction of 20%, adjusted for non-compliance/drop-out of 20%.

STUDY DESIGN This is a controlled, double-blind two-centre trial with 3090 included men and women who underwent coronary angiography at Haukeland University Hospital or Stavanger University Hospital between April 1999 and April 2004. At baseline about 1300 patients underwent PCI and 600 underwent CABG. The patients were randomized into 4 groups in a 2 x 2 factorial design to receive one of the following four treatments: A, folic acid 0.8 mg plus vitamin B12 0.4 mg and vitamin B6 40 mg per day; B, folic acid 0.8 mg plus vitamin B12 0.4 mg per day; C, vitamin B6 40 mg per day; D, placebo. The active drug and the placebo tablets had identical appearance and taste. Treatment was started as soon as the patients were randomized after the coronary angiography procedure. The patients have been undergoing interviews, clinical examination and blood-sampling at baseline, at follow-up after 1 month and 1 year, and at a final study visit. In addition, information on dietary habits was obtained from 2400 patients at baseline. Among 350 patients that have undergone PCI at baseline, a full clinical examination, blood sampling and repeat coronary angiography to assess re-stenosis has been performed about 9 (6-12) months after the PCI procedure. For these patients, angiograms suitable for quantitative coronary angiography (QCA) analysis have been obtained at the baseline and follow-up invasive procedures.

The follow-up was terminated ahead of schedule in October 2005 due to lack of compliance of the participants caused by media reports from the NORVIT study (NCT00266487) on potential increased cancer risk associated by B vitamin supplementation. The patients had then been followed for 1.5 - 5 years.

STUDY END POINTS Primary clinical endpoints during follow-up are all cause death, non-fatal acute myocardial infarction, acute hospitalization for unstable angina and non-fatal thromboembolic stroke (infarction). Secondary endpoints are fatal and non-fatal acute myocardial infarction (including procedure related myocardial infarction), acute hospitalization for angina, stable angina with angiographic verified progression, myocardial revascularization, fatal and non-fatal thromboembolic stroke.


Condition Intervention Phase
Coronary Artery Disease
Myocardial Infarction
Cerebrovascular Stroke
Drug: folic acid, vitamin B12 (cyanocobalamin), vitamin B6 (pyridoxine)
Drug: folic acid, vitamin B12 (cyanocobalamin)
Drug: vitamin B6 (pyridoxine)
Drug: placebo
Phase 3

Study Type: Interventional
Study Design: Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Factorial Assignment
Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor)
Primary Purpose: Prevention
Official Title: A Randomised Double Blind Study of the Effects of Homocysteine Lowering Therapy on Mortality and Cardiac Events in Patients Undergoing Coronary Angiography

Resource links provided by NLM:


Further study details as provided by Haukeland University Hospital:

Primary Outcome Measures:
  • Composite of all cause death, non-fatal acute myocardial infarction, acute hospitalization for unstable angina pectoris, and of non-fatal thromboembolic stroke (infarction) [ Time Frame: During follow-up, 1.5-5 years ] [ Designated as safety issue: No ]

Secondary Outcome Measures:
  • Fatal and non-fatal acute myocardial infarction, including procedure related myocardial infarction [ Time Frame: During follow-up, 1.5-5 years ] [ Designated as safety issue: No ]
  • Acute hospitalization for angina [ Time Frame: During follow-up, 1.5-5 years ] [ Designated as safety issue: No ]
  • Stable angina with angiographic verified progression [ Time Frame: During follow-up, 1.5-5 years ] [ Designated as safety issue: No ]
  • Myocardial revascularization [ Time Frame: During follow-up, 1.5-5 years ] [ Designated as safety issue: No ]
  • Fatal and non-fatal thromboembolic stroke [ Time Frame: During follow-up, 1.5-5 years ] [ Designated as safety issue: No ]
  • Cancer [ Time Frame: During follow-up, 1.5-5 years ] [ Designated as safety issue: Yes ]

Enrollment: 3096
Study Start Date: April 1999
Study Completion Date: February 2008
Primary Completion Date: June 2007 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Active Comparator: 1
folic acid (0.8 mg) plus vitamin B12 (0.4 mg) and vitamin B6 (40 mg)
Drug: folic acid, vitamin B12 (cyanocobalamin), vitamin B6 (pyridoxine)
folic acid 0.8 mg plus vitamin B12 0.4 mg and vitamin B6 40 mg, in a capsule, taken orally once a day
Active Comparator: 2
folic acid (0.8 mg) plus vitamin B12 (0.4 mg)
Drug: folic acid, vitamin B12 (cyanocobalamin)
folic acid 0.8 mg plus vitamin B12 0.4 mg, in a capsule, taken orally once a day
Active Comparator: 3
vitamin B6 (40 mg)
Drug: vitamin B6 (pyridoxine)
vitamin B6 40 mg, in a capsule, taken orally once a day
Placebo Comparator: 4
placebo
Drug: placebo
placebo, in a capsule, taken orally once a day

  Show Detailed Description

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • adults ≥ 18 years able to give informed consent
  • patients prepared to undergo long-term follow-up
  • patients with and without significant coronary artery disease (CAD) who have undergone coronary angiography just before inclusion

Exclusion Criteria:

  • patients who are not available for follow-up
  • patients who have previously participated in this study
  • patients with known alcohol abuse or serious mental illness
  • patients with known active malignant disease
  • patients who have undergone coronary angiography for specific reasons, i.e. assessment for cardiac transplantation, kidney donor, heart donor, diagnostic assessment of cardiomyopathy
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00354081

Locations
Norway
Department of Heart Disease, Haukeland University Hospital
Bergen, Norway, 5021
Department of Cardiology, Stavanger University Hospital
Stavanger, Norway, 4011
Sponsors and Collaborators
Haukeland University Hospital
The Research Council of Norway
Norwegian Foundation for Health and Rehabilitation
Norwegian Heart and Lung Patient Organisation
The Royal Norwegian Ministry of Health
Locus for Homocysteine and Related Vitamins, University of Bergen, Norway
Locus for Cardiac Research, University of Bergen, Norway
Foundation to Promote Research into Functional Vitamin B12 Deficiency, Bergen, Norway
Alpharma Pharmaceuticals LLC, a subsidiary of Pfizer Inc.
Investigators
Principal Investigator: Ottar Nygård, MD, PhD Haukeland University Hospital
  More Information

Publications:

Additional publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
Responsible Party: Haukeland University Hospital
ClinicalTrials.gov Identifier: NCT00354081     History of Changes
Other Study ID Numbers: NSD-14154
Study First Received: July 19, 2006
Last Updated: July 11, 2013
Health Authority: Norway: Norwegian Medicines Agency
Norway: Data Protection Authority
Norway: Norwegian Social Science Data Services

Keywords provided by Haukeland University Hospital:
Coronary Artery Disease
Myocardial Infarction
Cerebrovascular Stroke
Homocysteine
Folic Acid
Vitamin B 12
Vitamin B 6

Additional relevant MeSH terms:
Coronary Artery Disease
Coronary Disease
Myocardial Infarction
Stroke
Cerebral Infarction
Heart Diseases
Cardiovascular Diseases
Arterial Occlusive Diseases
Vascular Diseases
Cerebrovascular Disorders
Brain Diseases
Central Nervous System Diseases
Nervous System Diseases
Myocardial Ischemia
Infarction
Arteriosclerosis
Ischemia
Pathologic Processes
Necrosis
Brain Infarction
Brain Ischemia
Folic Acid
Vitamin B Complex
Hydroxocobalamin
Vitamin B 12
Pyridoxine
Vitamin B 6
Pyridoxal
Hematinics
Vitamins

ClinicalTrials.gov processed this record on April 16, 2014