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Vitamin D and Cardiac Autonomic Tone in Hemodialysis (VITAH)

Primary Purpose

Cardiovascular Disease, Sudden Cardiac Death

Status
Completed
Phase
Phase 2
Locations
Canada
Study Type
Interventional
Intervention
Alfacalcidol
Ergocalciferol
Sponsored by
University of Calgary
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Cardiovascular Disease focused on measuring vitamin D, hemodialysis, sudden cardiac death, heart rate variability, cardiac autonomic tone

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • age ≥ 18 years
  • 3x weekly hemodialysis outpatient within Calgary for at least 3 months prior to enrolment
  • physician consent to participate in VD supplementation regimen
  • ability and agreement to cease any VD medication for 4 weeks prior to initiation of study
  • able to comprehend study and provide oral and written consent in English

Exclusion Criteria:

  • any major cardiovascular event (new onset arrhythmia, hospitalization for a cardiac event) noted in patient chart within the 6 month period prior to initiation of the study
  • currently on VD therapy/refusal to cease VD therapy for 4 weeks prior to initiation of study
  • physician anticipates death or adverse event within the next year- known discharge from hemodialysis (transfer to peritoneal dialysis, kidney transplant)

Sites / Locations

  • Northland Hemodialysis Clinic
  • Foothills Medical Centre - University of Calgary
  • Sheldon M. Chumir Health Centre

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Vitamin D Sequence 1

Vitamin D Treatment Sequence 2

Arm Description

6 weeks - alfacalcidol 0.25mcg + placebo 3x per week, 12 week washout, 6 weeks - alfacalcidol 0.25mcg 3x per week + 50,000IU ergocalciferol 1x per week (placebo the 2 remaining days)

6 weeks - alfacalcidol 0.25mcg 3x per week + 50,000IU ergocalciferol 1x per week (placebo the 2 remaining days), 12 week washout, 6 weeks - alfacalcidol 0.25mcg + placebo 3x per week

Outcomes

Primary Outcome Measures

LF:HF
Low frequency to high frequency ratio (sympathetic vs. parasympathetic cardiac autonomic power)
LF:HF
Low frequency to high frequency ratio (sympathetic vs. parasympathetic cardiac autonomic power)
LF:HF
Low frequency to high frequency ratio (sympathetic vs. parasympathetic cardiac autonomic power)

Secondary Outcome Measures

SDNN
standard deviation of normal wave (heart rate variability time domain)
SDANN
standard deviation of the average normal wave (heart rate variability time domain)
pNN50%
percentage of normal waves which differ in frequency > 50 ms compared to the wave directly before (heart rate variability time domain)
LF
Low-frequency (ms squared and normalized units), thought to reflect sympathetic contribution from the cardiac autonomic nervous system
HF
High-frequency (ms squared and normalized units), thought to reflect parasympathetic contribution from the cardiac autonomic nervous system

Full Information

First Posted
January 17, 2013
Last Updated
August 29, 2016
Sponsor
University of Calgary
Collaborators
Alberta Innovates Health Solutions, Canadian Institutes of Health Research (CIHR)
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1. Study Identification

Unique Protocol Identification Number
NCT01774812
Brief Title
Vitamin D and Cardiac Autonomic Tone in Hemodialysis
Acronym
VITAH
Official Title
Vitamin D Supplementation and Cardiac Autonomic Tone in Hemodialysis Patients: A Blinded, Randomized-controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
August 2016
Overall Recruitment Status
Completed
Study Start Date
January 2013 (undefined)
Primary Completion Date
March 2015 (Actual)
Study Completion Date
March 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Calgary
Collaborators
Alberta Innovates Health Solutions, Canadian Institutes of Health Research (CIHR)

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Despite advances in treatment of conventional cardiovascular risk factors, patients with kidney disease remain at high risk for fatal cardiac events. To date, kidney disease affects approximately 2 million Canadians; however, this patient population remains grossly understudied due to the complex nature of the disease. The inadequacy of the literature to address the cardiovascular-related mortality rates in those with kidney disease reflects the urgent need for investigation of novel risk factors. One cardiovascular risk factor which has recently been validated is the clinical measurement of cardiac autonomic tone (CAT). CAT refers to the amount of activity contributed by the stimulatory and inhibitory limbs of the cardiac autonomic nervous system, which work in concert with one another to control heart rate. CAT can be quantified computer analysis of heart rate over time, captured by a simple Holter electrocardiogram (ECG) recording. Abnormal CAT, which occurs when the autonomic system does not control heart rate properly in response to physical demands or stress, is associated with risk of adverse cardiovascular events in both healthy and high risk populations. It has recently been shown that patients with severe kidney disease demonstrate significant CAT abnormalities, thus exaggerated susceptibility to cardiac death. Vitamin D (VD) deficiency is also common in this patient population due to the fact that the kidney plays a crucial role in VD metabolism. Given that VD deficiency is an established cardiovascular risk factor on its own, it is possible that kidney disease patients experienced compounded risk due to the combination of VD deficiency and abnormal CAT. However, no study has ever investigated whether VD deficiency influences CAT in healthy or diseased populations. To our knowledge, this will be the first trial to ever examine the effect, if any, of different VD supplementation treatments (standard of care vs. combination) on CAT in a population burdened with overwhelming risk and incidence of cardiovascular and sudden cardiac death risk.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cardiovascular Disease, Sudden Cardiac Death
Keywords
vitamin D, hemodialysis, sudden cardiac death, heart rate variability, cardiac autonomic tone

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 2
Interventional Study Model
Crossover Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
56 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Vitamin D Sequence 1
Arm Type
Active Comparator
Arm Description
6 weeks - alfacalcidol 0.25mcg + placebo 3x per week, 12 week washout, 6 weeks - alfacalcidol 0.25mcg 3x per week + 50,000IU ergocalciferol 1x per week (placebo the 2 remaining days)
Arm Title
Vitamin D Treatment Sequence 2
Arm Type
Active Comparator
Arm Description
6 weeks - alfacalcidol 0.25mcg 3x per week + 50,000IU ergocalciferol 1x per week (placebo the 2 remaining days), 12 week washout, 6 weeks - alfacalcidol 0.25mcg + placebo 3x per week
Intervention Type
Dietary Supplement
Intervention Name(s)
Alfacalcidol
Intervention Description
0.25 mcg 3x per week for 6 weeks
Intervention Type
Dietary Supplement
Intervention Name(s)
Ergocalciferol
Intervention Description
50,000IU 1x per week for 6 weeks
Primary Outcome Measure Information:
Title
LF:HF
Description
Low frequency to high frequency ratio (sympathetic vs. parasympathetic cardiac autonomic power)
Time Frame
change from baseline to 6 weeks
Title
LF:HF
Description
Low frequency to high frequency ratio (sympathetic vs. parasympathetic cardiac autonomic power)
Time Frame
change from 6 weeks to 18 weeks
Title
LF:HF
Description
Low frequency to high frequency ratio (sympathetic vs. parasympathetic cardiac autonomic power)
Time Frame
change from 18 weeks to 24 weeks
Secondary Outcome Measure Information:
Title
SDNN
Description
standard deviation of normal wave (heart rate variability time domain)
Time Frame
every 6 weeks up to 24 weeks
Title
SDANN
Description
standard deviation of the average normal wave (heart rate variability time domain)
Time Frame
every 6 weeks up to 24 weeks
Title
pNN50%
Description
percentage of normal waves which differ in frequency > 50 ms compared to the wave directly before (heart rate variability time domain)
Time Frame
every 6 weeks up to 24 weeks
Title
LF
Description
Low-frequency (ms squared and normalized units), thought to reflect sympathetic contribution from the cardiac autonomic nervous system
Time Frame
every 6 weeks up to 24 weeks
Title
HF
Description
High-frequency (ms squared and normalized units), thought to reflect parasympathetic contribution from the cardiac autonomic nervous system
Time Frame
every 6 weeks up to 24 weeks
Other Pre-specified Outcome Measures:
Title
25-hydroxy vitamin D
Time Frame
every 6 weeks up to 24 weeks
Title
1,25-dihydroxyvitamin D
Time Frame
every 6 weeks up to 24 weeks
Title
Parathyroid hormone
Time Frame
every 6 weeks up to 24 weeks
Title
Calcium
Time Frame
every 6 weeks up to 24 weeks
Title
Phosphate
Time Frame
every 6 weeks up to 24 weeks
Title
Pre- and post-dialysis weight
Time Frame
every 6 weeks up to 24 weeks
Title
Epinephrine
Time Frame
every 6 weeks up to 24 weeks
Title
Norepinephrine
Time Frame
every 6 weeks up to 24 weeks
Title
Renin-angiotensin system activity (circulating)
Description
renin, angiotensin II, aldosterone
Time Frame
every 6 weeks up to 24 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: age ≥ 18 years 3x weekly hemodialysis outpatient within Calgary for at least 3 months prior to enrolment physician consent to participate in VD supplementation regimen ability and agreement to cease any VD medication for 4 weeks prior to initiation of study able to comprehend study and provide oral and written consent in English Exclusion Criteria: any major cardiovascular event (new onset arrhythmia, hospitalization for a cardiac event) noted in patient chart within the 6 month period prior to initiation of the study currently on VD therapy/refusal to cease VD therapy for 4 weeks prior to initiation of study physician anticipates death or adverse event within the next year- known discharge from hemodialysis (transfer to peritoneal dialysis, kidney transplant)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Dr. Sofia B Ahmed, MD, MMSc
Organizational Affiliation
University of Calgary
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Dr. Derek Exner, MD, MPH
Organizational Affiliation
University of Calgary, Libin Cardiovascular Institute
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Dr. Brenda Hemmelgarn, MD, PhD, MN
Organizational Affiliation
University of Calgary
Official's Role
Principal Investigator
Facility Information:
Facility Name
Northland Hemodialysis Clinic
City
Calgary
State/Province
Alberta
ZIP/Postal Code
T2L 2J8
Country
Canada
Facility Name
Foothills Medical Centre - University of Calgary
City
Calgary
State/Province
Alberta
ZIP/Postal Code
T2N 2T9
Country
Canada
Facility Name
Sheldon M. Chumir Health Centre
City
Calgary
State/Province
Alberta
ZIP/Postal Code
T2R 0X7
Country
Canada

12. IPD Sharing Statement

Citations:
PubMed Identifier
22223455
Citation
Mann MC, Exner DV, Hemmelgarn BR, Turin TC, Sola DY, Ahmed SB. Impact of gender on the cardiac autonomic response to angiotensin II in healthy humans. J Appl Physiol (1985). 2012 Mar;112(6):1001-7. doi: 10.1152/japplphysiol.01207.2011. Epub 2012 Jan 5.
Results Reference
background
PubMed Identifier
20688781
Citation
Drechsler C, Pilz S, Obermayer-Pietsch B, Verduijn M, Tomaschitz A, Krane V, Espe K, Dekker F, Brandenburg V, Marz W, Ritz E, Wanner C. Vitamin D deficiency is associated with sudden cardiac death, combined cardiovascular events, and mortality in haemodialysis patients. Eur Heart J. 2010 Sep;31(18):2253-61. doi: 10.1093/eurheartj/ehq246. Epub 2010 Aug 5.
Results Reference
background
PubMed Identifier
18452777
Citation
Lahiri MK, Kannankeril PJ, Goldberger JJ. Assessment of autonomic function in cardiovascular disease: physiological basis and prognostic implications. J Am Coll Cardiol. 2008 May 6;51(18):1725-33. doi: 10.1016/j.jacc.2008.01.038.
Results Reference
background
PubMed Identifier
23752493
Citation
Mann MC, Exner DV, Hemmelgarn BR, Sola DY, Turin TC, Ellis L, Ahmed SB. Vitamin D levels are associated with cardiac autonomic activity in healthy humans. Nutrients. 2013 Jun 10;5(6):2114-27. doi: 10.3390/nu5062114.
Results Reference
background
PubMed Identifier
27690095
Citation
Mann MC, Exner DV, Hemmelgarn BR, Hanley DA, Turin TC, MacRae JM, Wheeler DC, Sola DY, Ramesh S, Ahmed SB. The VITAH Trial-Vitamin D Supplementation and Cardiac Autonomic Tone in Patients with End-Stage Kidney Disease on Hemodialysis: A Blinded, Randomized Controlled Trial. Nutrients. 2016 Sep 28;8(10):608. doi: 10.3390/nu8100608.
Results Reference
derived
PubMed Identifier
25098377
Citation
Mann MC, Exner DV, Hemmelgarn BR, Hanley DA, Turin TC, MacRae JM, Ahmed SB. The VITAH trial VITamin D supplementation and cardiac Autonomic tone in Hemodialysis: a blinded, randomized controlled trial. BMC Nephrol. 2014 Aug 6;15:129. doi: 10.1186/1471-2369-15-129.
Results Reference
derived

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Vitamin D and Cardiac Autonomic Tone in Hemodialysis

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