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Vitamin D Therapy to Reduce Cardiac Damage Among Vulnerable Hypertensive Patients

Adjunct Vitamin D Therapy as a Means to Reduce the Disparity in Subclinical Target Organ Cardiac Damage Among Vulnerable Hypertensive Patients

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01360476
Acronym
AdDReaCH
Enrollment
354
Registered
2011-05-25
Start date
2011-08-31
Completion date
2015-11-30
Last updated
2015-12-09

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

Conditions

Hypertension, Left Ventricular Hypertrophy

Keywords

hypertension, left ventricular hypertrophy, Vitamin D, African-Americans

Brief summary

This project seeks to reduce the disparity in hypertensive heart disease which exists for African-Americans who have poorly controlled hypertension (HTN), also known as blood pressure (BP). The investigators are targeting a highly vulnerable, often neglected subject population which stands to benefit tremendously from better BP control and a corresponding decrease in heart damage. HTN occurs early in life and more often in African-Americans, reducing both quality and quantity of life. Inner-city African-Americans with HTN utilize the emergency department (ED) for chronic BP management. Like cardiovascular disease, vitamin D deficiency disproportionately affects African-Americans. Vitamin D is thought to play an important role in cardiovascular health. Vitamin D replacement in those who are deficient has been thought to reduce the cardiovascular disease, especially if initiated early before irreversible damage has occurred, but this has yet to be tested in a prospective clinical trial. Accordingly, this proposal was designed to investigate the relationship between vitamin D and cardiac damage (as identified on cardiac magnetic resonance imaging) in a cohort of African-American, vitamin D deficient hypertensive patients without prior history of heart disease. The primary objective of this proposal is to evaluate the efficacy of vitamin D therapy in vitamin D deficient African-Americans with HTN. Vitamin D is an inexpensive treatment, which, if shown to be effective could improve the existing approach to a widely accessible, cost-effective option.

Interventions

DIETARY_SUPPLEMENTcholecalciferol (Vitamin D)

50,000 UI, chewable wafer every 2 weeks for 52 weeks (27 total doses)

DIETARY_SUPPLEMENTPlacebo

chewable wafer every 2 weeks for 52 weeks (27 total doses)

Sponsors

National Institute on Minority Health and Health Disparities (NIMHD)
CollaboratorNIH
Wayne State University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
30 Years to 74 Years
Healthy volunteers
No

Inclusion criteria

* Individuals with known HTN * African-American race (self reported) * Repeat SBP ≥ 160 mmHg within 1 hour of arrival * Age 30-74 years * Asymptomatic state (class I as defined by Goldman Specific Activity Scale)

Exclusion criteria

* Dyspnea (exertional, rest or nocturnal) or chest pain as a primary or secondary chief complaint * Prior history of HF, coronary artery disease, myocardial infarction, cardiomyopathy (any), valvular heart disease (any) or renal failure with current, previous, or planned future dialysis * Acute illness or injury which necessitates hospital admission * Acute alcohol or cocaine intoxication or history of chronic alcohol (determined using the CAGE screening questions) or cocaine (self-reported) abuse * Acute or decompensated psychiatric disorder or any underlying psychiatric disorder or cognitive deficit which precludes effective on-going communication or ability to follow-up as required * Cancer (other than skin), HIV, or any other medical condition that might limit life expectancy * Hepatitis or liver enzyme (ALT, AST) elevations \> 1.5x normal * Planned move \> 50 miles in the next 9 months * History of kidney stones * GFR \<30 * Serum calcium \> 10.5 mg/dl or known history of hypercalcemia * History of or known primary hyperparathyroidism * Sarcoidosis or other granulomatous disease * Pregnant or planning to become pregnant * Allergy or known hypersensitivity to gadolinium contrast * Severe claustrophobia

Design outcomes

Primary

MeasureTime frameDescription
Change from Baseline in left ventricular hypertrophy at 1 yearbaseline, 16weeks, 52weeksCardiac MRI will be used to assess this change.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 11, 2026