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How Does Magnesium Status Influence Calcium Homeostasis?

How Does Magnesium Status Influence Calcium Homeostasis?

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01593501
Enrollment
39
Registered
2012-05-08
Start date
2012-05-31
Completion date
2014-08-31
Last updated
2016-11-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Calcium Metabolism Disorders, Magnesium Deficiency

Keywords

vitamin D, cholecalciferol, bone mineral density, Magnesium deficiency, Calcium metabolism disorders

Brief summary

The investigators aim to recruit 60 women who have agreed to participate in an existing randomized, double-blind, placebo-controlled trial (Treatment of Vitamin D Insufficiency, HSC 2009-0055). In this trial, the investigators propose to evaluate the associations between magnesium intake, magnesium stores, fractional magnesium absorption and calcium homeostasis. The investigators will stratify 60 subjects in the sub-study, ensuring that approximately 20 subjects are randomized into each treatment arm (placebo, low-dose and high-dose vitamin D). The investigators already assess calcium homeostasis throughout the study by measuring bone mineral density, fractional calcium absorption, serum and urine calcium levels, among other tests. In the sub-study of 60 women, the investigators will evaluate whether habitually higher magnesium intake increases or decreases fractional calcium absorption. The investigators will evaluate the interplay between magnesium stores, vitamin D levels and serum parathyroid hormone levels. The investigators will directly assess magnesium stores using serum magnesium and 24-hour urine magnesium levels, and will measure magnesium absorption using the dual stable isotope approach.

Detailed description

Use of serum magnesium isotopes to measure fractional magnesium absorption Four day food diaries to assess magnesium intake Standard urine and serum chemistries for remaining labs as noted above

Interventions

DIETARY_SUPPLEMENTvitamin D3

pharmaceutical grade D3

Sponsors

National Institutes of Health (NIH)
CollaboratorNIH
National Institute on Aging (NIA)
CollaboratorNIH
University of Wisconsin, Madison
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
FEMALE
Age
30 Years to 75 Years
Healthy volunteers
Yes

Inclusion criteria

* participants eligible for the study Treatment of vitamin D insufficiency are eligible for participation in the current sub-study

Exclusion criteria

* identical to those covered in HSC #2009-0055

Design outcomes

Primary

MeasureTime frameDescription
Evaluate the associations between magnesium intake, magnesium stores, fractional magnesium absorption and calcium homeostasis.0-12 monthsTo evaluate relationships between magnesium intake and fractional magnesium absorption at baseline and 12 months, among 60 women participating in HSC Protocol 2009-0055, and to assess whether vitamin D therapy influences magnesium absorption among these women. We will also evaluate whether data collected from less than 72 hours of urine following tracer administration permits accurate assessment of fractional magnesium absorption.

Secondary

MeasureTime frameDescription
Does vitamin D therapy have a differential impact on calcium absorption that is dependent on magnesium stores?0-12 monthsTo assess whether vitamin D therapy has a differential impact on calcium absorption, depending on magnesium stores. We will use data from all subjects participating in HSC Protocol 2009-0055 to evaluate whether magnesium status is a co-factor in the change in calcium absorption that occurs with vitamin D therapy.
Assessing relationships between magnesium status and bone mineral density.0-12 months
Evaluate how magnesium status impacts the relationship between vitamin D levels and parathyroid hormone levels.0-12 months

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026