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A Trial of Thiamin Supplementation in Patients With Heart Failure

Primary Purpose

Heart Failure

Status
Completed
Phase
Phase 4
Locations
Canada
Study Type
Interventional
Intervention
Vitamin B1
Placebo
Sponsored by
Unity Health Toronto
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Heart Failure focused on measuring Thiamin supplementation, Thiamin deficiency, Heart failure, Improve heart function, Vitamin B1 supplementation

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • primary diagnosis of ischemic, dilated, idiopathic or valvular heart failure characterized by an ejection fraction of < 45% (echocardiography or radionuclide scan)
  • have an optimized medication regimen (ACE inhibitor or angiotensin receptor blocker, and beta blocker at target doses, or up-titrated to the maximum doses as tolerated)
  • been stable (on current medication regimen with no hospitalizations for acute decompensated heart failure > 2 months) prior to entry into the study

Exclusion Criteria: Participants will be excluded if they are:

  • unable or unwilling to provide informed consent
  • have any concurrent condition which would result in thiamin deficiency, namely gastrointestinal disorders, magnesium deficiency, liver disease, thyrotoxicosis, B12 deficiency, folate deficiency, prolonged diarrhoeal disease, dialysis, prolonged fever or infection, recent myocardial infarction, coronary revascularization (percutaneous coronary intervention or coronary artery bypass surgery within 3 months), or renal failure
  • are rapidly deteriorating, who are not on a stable medication regimen (2 months or more) or who have been hospitalized for acute decompensated heart failure in the last 2 months
  • are on experimental medications
  • are taking vitamin supplements containing thiamin >10mg/day
  • consume excessive alcohol (> 3 drinks per day), have a documented history of alcoholism or have documented alcoholic cardiomyopathy
  • have permanent atrial fibrillation
  • are pregnant or would like to become pregnant
  • have a right-to-left, bidirectional, or transient right to left cardiac shunts
  • have clinically suspected wet Beri Beri in the opinion of the treating physician

Sites / Locations

  • Niagara North Family Health Team

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Oral thiamin supplementation

Sugar pill

Arm Description

Vitamin B1 (Oral thiamin) 100mg BID for 6 months

oral placebo 1 tablet BID for 6 months

Outcomes

Primary Outcome Measures

Left ventricular ejection fraction measured by CMR or 3D echo at 6 months

Secondary Outcome Measures

LV volume, regional function as measure by CMR tagging
Exercise tolerance - distance walked in the standard six-minute walk test
Levels of circulating BNP, norepinephrine and F2-isoprostanes
Scores on the Living with Heart Failure quality of life instrument
Prevalence of TD in an ambulatory HF population

Full Information

First Posted
August 13, 2009
Last Updated
February 26, 2018
Sponsor
Unity Health Toronto
Collaborators
Heart and Stroke Foundation of Ontario
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1. Study Identification

Unique Protocol Identification Number
NCT00959075
Brief Title
A Trial of Thiamin Supplementation in Patients With Heart Failure
Official Title
A Randomized Controlled Trial of the Effect of Thiamin Supplementation on Heart Function in Ambulatory Patients With Heart Failure
Study Type
Interventional

2. Study Status

Record Verification Date
February 2018
Overall Recruitment Status
Completed
Study Start Date
September 2009 (undefined)
Primary Completion Date
November 2015 (Actual)
Study Completion Date
November 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Unity Health Toronto
Collaborators
Heart and Stroke Foundation of Ontario

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Background: Patients with heart failure (HF) are at increased risk of developing thiamin deficiency (TD). Thiamin (vitamin B1) is required for the production of energy and therefore TD may contribute to the energy depletion commonly observed in the failing heart. Thiamin supplementation trials to date have shown conflicting results and therefore further studies to explain the impact of thiamin supplementation on HF patients with TD is necessary. Objective: The purpose of this study is to determine whether thiamin supplementation in an ambulatory cohort of patients with systolic heart failure will provide any benefit in terms of improved heart function, symptoms, exercise capacity, and quality of life. Description: Patients involved in the study will be given either thiamin supplements or a matching placebo (pills containing no thiamin) for 6 months. The ability of the heart to pump before and after the supplementation will be measured using cardiac magnetic resonance imaging (MRI)and/or 3D echocardiography. Relevance: This study will determine whether thiamin supplementation improves cardiac function, exercise tolerance and quality of life. Thiamin supplementation is widely available, inexpensive, and safe. Therefore this trial may have a major impact on the optimal management of the expanding population of heart failure patients.
Detailed Description
Background: There is now accumulating evidence that patients with heart failure (HF) have a high prevalence of thiamin deficiency (TD). Since thiamin is a key cofactor in the enzyme systems that produce energy from both carbohydrates and fats, TD may contribute to the energy depletion frequently observed in the failing heart. Altered energy reserves with a reduction in myocardial ATP have now been recognized to play a critical role in the development and progression of HF. Therefore, correction of TD may enhance cardiac energy substrate availability and utilization, leading to improvement of ventricular function and symptoms. Primary Hypothesis: The left ventricular ejection fraction in stable, ambulatory patients with systolic heart failure receiving 6 months of oral thiamin supplementation will be significantly higher in comparison with those receiving a placebo. Secondary Hypothesis: In heart failure patients oral thiamin supplementation will 1)have favourable effects on ventricular remodelling (reduction in diastolic and systolic volumes) and regional function; 2)reduce neurohormonal stimulation (BNP and norepinephrine) as well as oxidative stress; 3)improve exercise capacity and 4)improve symptoms and quality of life. Ambulatory patients attending heart failure clinics at Mount Sinai, University Health Network, Trillium Health Centre and St. Michael's Hospital with systolic heart failure (NYHA class II-IV, left ventricular ejection fraction <45%) will be screened for eligibility to participate in our randomized trial. We will randomize seventy eligible patients using a stratified, permuted block randomization scheme, to be given either 100mg BID of thiamin HCl or a matching placebo BID in a 1:1 ratio to be taken for six months. All study personnel will be blinded to treatment assignment. Participants will have baseline and follow-up visits which include collecting demographic data, history of medication use, symptoms, anthropometrics as well as a physical exam. Left ventricular ejection fraction, volumes, and regional function will be measured using a standardized echocardiogram and cardiac MRI at baseline and after six months of supplementation. At this time, blood markers of thiamin status, oxidative stress (F2 isoprostanes) and neurohormonal activation (norepinephrine and BNP) will also be measured. Participants will also complete a six-minute walk test, a 3-day dietary record, the Living with Heart Failure quality of life instrument and a 24-hour urine collection (to measure urinary thiamin excretion) at both baseline and follow-up visits. Compliance will be measured using returned pill counts and verified by measuring plasma thiamin levels which respond rapidly to thiamin supplementation.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Heart Failure
Keywords
Thiamin supplementation, Thiamin deficiency, Heart failure, Improve heart function, Vitamin B1 supplementation

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
70 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Oral thiamin supplementation
Arm Type
Experimental
Arm Description
Vitamin B1 (Oral thiamin) 100mg BID for 6 months
Arm Title
Sugar pill
Arm Type
Placebo Comparator
Arm Description
oral placebo 1 tablet BID for 6 months
Intervention Type
Dietary Supplement
Intervention Name(s)
Vitamin B1
Other Intervention Name(s)
Jamieson - Thiamin Mononitrate
Intervention Description
100 mg Twice a day
Intervention Type
Dietary Supplement
Intervention Name(s)
Placebo
Intervention Description
Sugar pill
Primary Outcome Measure Information:
Title
Left ventricular ejection fraction measured by CMR or 3D echo at 6 months
Time Frame
6 months
Secondary Outcome Measure Information:
Title
LV volume, regional function as measure by CMR tagging
Time Frame
6 months
Title
Exercise tolerance - distance walked in the standard six-minute walk test
Time Frame
6 months
Title
Levels of circulating BNP, norepinephrine and F2-isoprostanes
Time Frame
6 months
Title
Scores on the Living with Heart Failure quality of life instrument
Time Frame
6 months
Title
Prevalence of TD in an ambulatory HF population
Time Frame
6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: primary diagnosis of ischemic, dilated, idiopathic or valvular heart failure characterized by an ejection fraction of < 45% (echocardiography or radionuclide scan) have an optimized medication regimen (ACE inhibitor or angiotensin receptor blocker, and beta blocker at target doses, or up-titrated to the maximum doses as tolerated) been stable (on current medication regimen with no hospitalizations for acute decompensated heart failure > 2 months) prior to entry into the study Exclusion Criteria: Participants will be excluded if they are: unable or unwilling to provide informed consent have any concurrent condition which would result in thiamin deficiency, namely gastrointestinal disorders, magnesium deficiency, liver disease, thyrotoxicosis, B12 deficiency, folate deficiency, prolonged diarrhoeal disease, dialysis, prolonged fever or infection, recent myocardial infarction, coronary revascularization (percutaneous coronary intervention or coronary artery bypass surgery within 3 months), or renal failure are rapidly deteriorating, who are not on a stable medication regimen (2 months or more) or who have been hospitalized for acute decompensated heart failure in the last 2 months are on experimental medications are taking vitamin supplements containing thiamin >10mg/day consume excessive alcohol (> 3 drinks per day), have a documented history of alcoholism or have documented alcoholic cardiomyopathy have permanent atrial fibrillation are pregnant or would like to become pregnant have a right-to-left, bidirectional, or transient right to left cardiac shunts have clinically suspected wet Beri Beri in the opinion of the treating physician
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mary E. Keith, PhD, RD
Organizational Affiliation
Unity Health Toronto
Official's Role
Principal Investigator
Facility Information:
Facility Name
Niagara North Family Health Team
City
St. Catharines
State/Province
Ontario
ZIP/Postal Code
L2R 1R5
Country
Canada

12. IPD Sharing Statement

Citations:
PubMed Identifier
31504093
Citation
Keith M, Quach S, Ahmed M, Azizi-Namini P, Al-Hesayen A, Azevedo E, James R, Leong-Poi H, Ong G, Desjardins S, Lee PJ, Ravamehr-Lake D, Yan AT. Thiamin supplementation does not improve left ventricular ejection fraction in ambulatory heart failure patients: a randomized controlled trial. Am J Clin Nutr. 2019 Dec 1;110(6):1287-1295. doi: 10.1093/ajcn/nqz192.
Results Reference
derived

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A Trial of Thiamin Supplementation in Patients With Heart Failure

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