The Effects of Vitamin D Repletion in Vitamin D Deficient Patients With Stage 3 and 4 Chronic Kidney Disease
- Conditions
- ProteinuriaChronic Renal Insufficiency
- Interventions
- Other: Placebo
- Registration Number
- NCT01029002
- Lead Sponsor
- Albert Einstein College of Medicine
- Brief Summary
A randomized clinical trial to determine if vitamin D repletion in CKD (Chronic Kidney Disease) patients with low vitamin D levels will decrease proteinuria, a marker of kidney damage.
- Detailed Description
This RCT will enroll 74 subjects, men and women over age of 18, with stage 3-4 CKD from various causes including diabetes and hypertension. Patients will be recruited from the Montefiore Medical Center Nephrology clinics and the Montefiore Medical Center internal medicine clinics and other interested individuals.
Informed consent will be obtained on all subjects. All subjects with meet with one of the investigators who will verbally explain to them the purpose of the study and the alternatives.
Blood and urine tests will be collected to assess for proteinuria, vitamin D levels, serum creatinine, calcium and phosphorus, as well as a urine albumin, calcium and creatinine. These tests will be used for experimental purposes only and will be collected at each study visit over the span of 6 months.
There will be two arms, an arm randomized to 50000IU of ergocalciferol once weekly and a placebo arm for 3 months. For an additional 3 months, all patients will be repleted with Vitamin D via open-label extension, based on their levels after 3 months.
Secondary outcomes include ambulatory blood pressure monitoring, hemoglobin A1c, HOMA-IR.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 74
- Age >18 years
- Ability to provide informed consent
- Chronic kidney disease stage 3 and 4
- On ACE inhibitor or ARB for albuminuria if tolerated
- Assessed during eligibility screen:
- Albuminuria >30 mg/g creatinine
- 25(OH) vitamin D level >12.5 and <75 nmol/L
- On vitamin D in past 4 weeks
- Plans to relocate out of New York City in the next 6 months
- 25 (OH) Vitamin D level <12.5 nmol/L
- HIV infection
- History of hypercalcemia or kidney stones
- Serum phosphate >5.5 mg/dl in past 3 months
- Serum calcium >10.0 mg/dl in past 3 months
- SBP >160 DBP >100 at screening visit
- Transplanted organ
- Cancer
- Polycystic kidney disease
- Rapidly deteriorating kidney function with the expectation for initiation of dialysis in less than 6 months
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Placebo Placebo Patients randomized to this arm will receive a placebo pill once weekly. Vitamin D 50000 IU Vitamin D Patients randomized to this arm will receive 50,000 IU of ergocalciferol in one unmarked pill once weekly.
- Primary Outcome Measures
Name Time Method Effect of Vitamin D Supplementation on Albuminuria in CKD Patients as Assessed by Urine Albumin/Creatinine Measures. 3 months Urine albumin and creatinine were measured on spot urine specimens.
- Secondary Outcome Measures
Name Time Method Effect of Repletion Doses of Vitamin D Increase 25(OH) Vitamin D Levels to Above 30 ng/mL in a Multi-ethnic Sample of Patients With CKD as a Secondary Outcome. 3 months 25(OH) vitamin D levels were measured using liquid chromatography.
Effect of Vitamin D Supplementation on Mean Systolic Blood Pressure as Measured by Ambulatory Blood Pressure in CKD Patients as a Secondary Outcome. 3 months
Trial Locations
- Locations (1)
Montefiore medical center
🇺🇸Bronx, New York, United States