A Study on the Impact of Calcium on Woman's Vascular Health
Primary Purpose
Cardiovascular Diseases, Osteoporosis
Status
Completed
Phase
Phase 4
Locations
Canada
Study Type
Interventional
Intervention
Calcium Citrate
Low Dietary Calcium
High Dietary Calcium
Sponsored by
About this trial
This is an interventional prevention trial for Cardiovascular Diseases focused on measuring Calcium Supplements, Dairy Foods, Cardiovascular Diseases, Osteoporosis, Postmenopause, Vitamin D, Micronutrients, Primary Prevention, Bone Health
Eligibility Criteria
Inclusion Criteria:
- Women aged 50 or more
- 2 years since last menstrual period
- Body Mass Index between 20 and 35 kg/m2
Exclusion Criteria:
- Atrial Fibrillation
- Coronary artery disease
- Myocardial infarction
- Stroke
- Transient ischaemic attack
- Peripheral vascular disease
- Sleep apnea
- Hypertension
- Hyperlipidemia
- Hyperparathyroidism
- Urinary tract lithiasis
- Rheumatoid arthritis
- Crohn's disease
- Ulcerative colitis
- Short gut syndrome
- Celiac disease
- Diabetes
- Cancer (any other than basal cell cancer of the skin)
- Pre-eclampsia
- Smoked in the last 5 years
- Cocaine use in the last year
- Consumption of more than 9 alcoholic drinks per week
- Chronic NSAID use
- Use of oral glucocorticoids or HRT (excluding vaginal preparations) in the last 2 years
- Use of anti-osteoporosis medications (bisphosphonates, selective estrogen-receptor modulators, denosumab, teriparatide, or calcitonin) in the last 3 years or anti-osteoporosis therapy which ended more than 3 years ago and whose duration was ≥ 5 years, or a fracture of the spine, shoulder, or hip was sustained while therapy
- Use of calcium and vitamin D supplements (including multivitamins and calcium-containing antacids) in the last 2 months
- High 10-year probability of major osteoporotic fracture (FRAX without BMD > 20%)
Sites / Locations
- Department of Internal Medicine; Montreal General Hospital
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Active Comparator
Active Comparator
No Intervention
Arm Label
Supplemental Calcium
Dietary Calcium
Usual Diet
Arm Description
750 mg Calcium Citrate per day 800 IU Vitamin D3 per day Low Dietary Calcium (450 mg per day)
400 IU Vitamin D3 per day High Dietary Calcium (1200 mg per day)
400 IU Vitamin D3 per day Unrestricted Dietary Calcium
Outcomes
Primary Outcome Measures
Vascular System
Measured as changes in:
Arterial stiffness (carotid-femoral pulse wave velocity)
Arterial wall thickness (carotid intima-media thickness)
Secondary Outcome Measures
Hemodynamics
Measured as changes in:
- Peripheral blood pressure
Full Information
NCT ID
NCT01731340
First Posted
November 16, 2012
Last Updated
September 16, 2019
Sponsor
McGill University Health Centre/Research Institute of the McGill University Health Centre
1. Study Identification
Unique Protocol Identification Number
NCT01731340
Brief Title
A Study on the Impact of Calcium on Woman's Vascular Health
Official Title
The Effect of Dietary Calcium Intake as Compared to Calcium Supplementation on Vascular Health and Bone Health in Postmenopausal Women
Study Type
Interventional
2. Study Status
Record Verification Date
September 2019
Overall Recruitment Status
Completed
Study Start Date
June 2012 (Actual)
Primary Completion Date
November 14, 2018 (Actual)
Study Completion Date
November 14, 2018 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
McGill University Health Centre/Research Institute of the McGill University Health Centre
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
The overarching aim of this randomized clinical trial is to estimate the effect of dietary intake of calcium as compared to supplemental calcium on the vascular system and markers of vascular and bone health in postmenopausal women.
Detailed Description
Calcium and vitamin D are essential nutrients for optimal bone health throughout life. Research has shown that postmenopausal women who consume appropriate amounts of these nutrients have better bone strength and fewer fractures than those who don't. However, researchers have recently questioned the safety of calcium and vitamin D obtained through supplements as they might increase the risk of cardiovascular events such as heart attacks and strokes.
The investigators propose to estimate the effect of dietary intake of calcium as compared to supplemental calcium on vascular and bone health in postmenopausal women.
Eligible participants will be assigned by chance (like a coin toss) to one of three groups: (1) 1200 mg of calcium from dietary sources and 1 capsule of 400 IU vitamin D supplement everyday after the first meal of the day; (2) 450 mg of calcium from dietary sources, 2 tablets of 250 mg calcium citrate supplement and 1 capsule of 800 IU vitamin D supplement everyday after the first meal of the day and 1 tablet of 250 mg calcium citrate supplement after the evening meal or snack; or (3) unrestricted calcium from dietary sources and 1 capsule of 400 IU vitamin D supplement everyday after the first meal of the day. Participants have an equal chance of being assigned to any of these three groups until 26 participants have been assigned to group (3). At this time participants will continue to be assigned by chance to either of the two remaining groups only.
Participants will also attend appointments at the Montreal General Hospital every 6-months where they will undergo anthropometric measurements, blood tests, urine tests, non-invasive ultrasounds to measure arterial stiffness and questionnaires. The questionnaires ask about health; lifestyle habits such as physical exercise, diet, and smoking; use of medications and dietary supplements; family history of illness, and past medical diagnoses. Participants will also receive monthly phone calls from study staff to monitor for adverse events and adherence.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cardiovascular Diseases, Osteoporosis
Keywords
Calcium Supplements, Dairy Foods, Cardiovascular Diseases, Osteoporosis, Postmenopause, Vitamin D, Micronutrients, Primary Prevention, Bone Health
7. Study Design
Primary Purpose
Prevention
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
123 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Supplemental Calcium
Arm Type
Active Comparator
Arm Description
750 mg Calcium Citrate per day
800 IU Vitamin D3 per day
Low Dietary Calcium (450 mg per day)
Arm Title
Dietary Calcium
Arm Type
Active Comparator
Arm Description
400 IU Vitamin D3 per day
High Dietary Calcium (1200 mg per day)
Arm Title
Usual Diet
Arm Type
No Intervention
Arm Description
400 IU Vitamin D3 per day
Unrestricted Dietary Calcium
Intervention Type
Dietary Supplement
Intervention Name(s)
Calcium Citrate
Intervention Description
750mg
Intervention Type
Other
Intervention Name(s)
Low Dietary Calcium
Intervention Description
450 mg
Intervention Type
Other
Intervention Name(s)
High Dietary Calcium
Intervention Description
1200 mg
Primary Outcome Measure Information:
Title
Vascular System
Description
Measured as changes in:
Arterial stiffness (carotid-femoral pulse wave velocity)
Arterial wall thickness (carotid intima-media thickness)
Time Frame
12 months
Secondary Outcome Measure Information:
Title
Hemodynamics
Description
Measured as changes in:
- Peripheral blood pressure
Time Frame
12 Months
Other Pre-specified Outcome Measures:
Title
Blood Biomarkers
Description
Measured as changes in:
Vascular health biomarkers
Bone health biomarkers
Time Frame
12 months
Title
Anthropomorphic measurements
Description
Measured as changes in bone health biomarkers.
Body mass index
Waist circumference
Body fat %
Time Frame
12 months
Title
Adverse Events
Description
Occurrence of cardiovascular, cerebrovascular and renal events as well as fractures and intolerance to interventions.
Time Frame
12 months
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Women aged 50 or more
2 years since last menstrual period
Body Mass Index between 20 and 35 kg/m2
Exclusion Criteria:
Atrial Fibrillation
Coronary artery disease
Myocardial infarction
Stroke
Transient ischaemic attack
Peripheral vascular disease
Sleep apnea
Hypertension
Hyperlipidemia
Hyperparathyroidism
Urinary tract lithiasis
Rheumatoid arthritis
Crohn's disease
Ulcerative colitis
Short gut syndrome
Celiac disease
Diabetes
Cancer (any other than basal cell cancer of the skin)
Pre-eclampsia
Smoked in the last 5 years
Cocaine use in the last year
Consumption of more than 9 alcoholic drinks per week
Chronic NSAID use
Use of oral glucocorticoids or HRT (excluding vaginal preparations) in the last 2 years
Use of anti-osteoporosis medications (bisphosphonates, selective estrogen-receptor modulators, denosumab, teriparatide, or calcitonin) in the last 3 years or anti-osteoporosis therapy which ended more than 3 years ago and whose duration was ≥ 5 years, or a fracture of the spine, shoulder, or hip was sustained while therapy
Use of calcium and vitamin D supplements (including multivitamins and calcium-containing antacids) in the last 2 months
High 10-year probability of major osteoporotic fracture (FRAX without BMD > 20%)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Suzanne Morin, MD MSc
Organizational Affiliation
McGill University Hospital Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Department of Internal Medicine; Montreal General Hospital
City
Montreal
State/Province
Quebec
ZIP/Postal Code
H3G 1A4
Country
Canada
12. IPD Sharing Statement
Plan to Share IPD
No
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A Study on the Impact of Calcium on Woman's Vascular Health
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