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Does vitamin D reduce blood pressure and left ventricular (LV) mass in resistant hypertensive patients with vitamin D insufficiency?

Does vitamin D reduce blood pressure and left ventricular (LV) mass in resistant hypertensive patients with vitamin D insufficiency? A double-blind, placebo-controlled, parallel-group randomised trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN63688695
Enrollment
74
Registered
2008-04-21
Start date
2009-01-01
Completion date
Unknown
Last updated
2017-11-27

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

Conditions

Hypertension Circulatory System Essential (primary) hypertension

Interventions

100,000 units of oral vitamin D3 every two months or placebo. Total treatment duration: 4 months Total follow up: 6 months

Sponsors

University of Dundee
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Aged greater than 18 years, either sex 2. Serum 25-hydroxy vitamin D less than 75 nmol/L 3. Office blood pressure (BP) greater than 140/90 mmHg despite three or more anti-hypertensives

Exclusion criteria

Exclusion criteria: 1. Hypertension known to be due to a correctable underlying medical or surgical cause 2. Estimated glomerular filtration rate less than 40 ml/min (by four variable Modification of Diet in Renal Disease [MDRD] equations) 3. Liver function tests (alanine aminotransferase [ALT], bilirubin, alkaline phosphatase) greater than 3 x normal 4. Corrected calcium greater than 2.60 mmol/L or less than 2.15 mmol/L 5. Known metastatic malignancy or sarcoidosis 6. Clinical diagnosis of osteomalacia 7. History of renal calculi 8. Diagnosis of heart failure with left ventricular systolic dysfunction 9. Atrial fibrillation 10. Already taking vitamin D supplements. Consumption of fish oils will not be a contra-indication to enrolment 11. Unable to give written informed consent 12. Pregnant or of childbearing age and not taking reliable contraception

Design outcomes

Primary

MeasureTime frame
Office BP, measured at 0, 2, 4 and 6 months

Secondary

MeasureTime frame
LV mass index, measured by cardiac magnetic resonance imaging [MRI] at 0 and 6 months

Countries

United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026