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Effect of Vitamin D3 on Cardiovascular Risk Factors

Effect of Vitamin D3 on Cardiovascular Risk Factors: a Randomized Trial in Human

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01501916
Enrollment
250
Registered
2011-12-30
Start date
2012-12-31
Completion date
2013-12-31
Last updated
2018-10-11

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

Conditions

Deficiency of Vitamin D3, Hypertensive Disease

Brief summary

The aim of this study is to investigate whether a supplementation of Vitamin D3 can be used to reduce atherosclerotic risk factors.

Detailed description

It is the objective of this study to investigate whether a supplementation with Vitamin D3 can be used to reduce atherosclerotic risk factors such as hypertension, inflammation and hyperlipidemia. The research question is whether Vitamin D3 can lower blood pressure in mildly hypertensive subjects who are naive to antihypertensive medication, whether Vitamin D reduces the level of systemic inflammation and whether Vitamin D3 has an effect on blood lipids. major outcomes: \- decrease of systolic blood pressure in the treatment group in comparison with the placebo group

Interventions

DIETARY_SUPPLEMENTVitamin D3

daily dosage of 50 µg Vitamin D3 for 8 weeks

DIETARY_SUPPLEMENTPlacebo

daily intake of placebo

Sponsors

German Federal Ministry of Education and Research
CollaboratorOTHER_GOV
Martin-Luther-Universität Halle-Wittenberg
Lead SponsorOTHER

Study design

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

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* human volunteers with mild hypertension

Exclusion criteria

* use of antihypertensive medication * use of vitamin d or calcium supplements * known renal, inflammatory or malignant diseases * hypercalcemia or hypercalciuria * participation in other clinical studies * use of tanning booths during the study

Design outcomes

Primary

MeasureTime frameDescription
blood pressureafter 8 weeks of supplementationmajor outcome variable is the decrease oy systolic blood pressure in the treatment group in comparison with the placebo group.

Outcome results

None listed

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