The Effects of Vitamin D Repletion in Vitamin D Deficient Patients With Stage 3 and 4 Chronic Kidney Disease
Primary Purpose
Chronic Renal Insufficiency, Proteinuria
Status
Completed
Phase
Phase 3
Locations
United States
Study Type
Interventional
Intervention
Vitamin D
Placebo
Sponsored by
About this trial
This is an interventional treatment trial for Chronic Renal Insufficiency focused on measuring Vitamin D, CKD, proteinuria
Eligibility Criteria
Inclusion Criteria:
- 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
Exclusion Criteria:
- 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
Sites / Locations
- Montefiore medical center
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
Vitamin D 50000 IU
Placebo
Arm Description
Patients randomized to this arm will receive 50,000 IU of ergocalciferol in one unmarked pill once weekly.
Patients randomized to this arm will receive a placebo pill once weekly.
Outcomes
Primary Outcome Measures
Effect of Vitamin D Supplementation on Albuminuria in CKD Patients as Assessed by Urine Albumin/Creatinine Measures.
Urine albumin and creatinine were measured on spot urine specimens.
Secondary Outcome Measures
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.
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.
Full Information
NCT ID
NCT01029002
First Posted
December 7, 2009
Last Updated
August 14, 2023
Sponsor
Albert Einstein College of Medicine
Collaborators
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
1. Study Identification
Unique Protocol Identification Number
NCT01029002
Brief Title
The Effects of Vitamin D Repletion in Vitamin D Deficient Patients With Stage 3 and 4 Chronic Kidney Disease
Official Title
The Effects of Vitamin D Repletion in Vitamin D Deficient Patients With Stage 3 and 4 Chronic Kidney Disease
Study Type
Interventional
2. Study Status
Record Verification Date
August 2023
Overall Recruitment Status
Completed
Study Start Date
October 2009 (undefined)
Primary Completion Date
June 2014 (Actual)
Study Completion Date
June 2014 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Albert Einstein College of Medicine
Collaborators
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
4. Oversight
Data Monitoring Committee
No
5. Study Description
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.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Renal Insufficiency, Proteinuria
Keywords
Vitamin D, CKD, proteinuria
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
74 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Vitamin D 50000 IU
Arm Type
Experimental
Arm Description
Patients randomized to this arm will receive 50,000 IU of ergocalciferol in one unmarked pill once weekly.
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Patients randomized to this arm will receive a placebo pill once weekly.
Intervention Type
Drug
Intervention Name(s)
Vitamin D
Intervention Description
Vitamin D, ergocalciferol, 50000 IU, weekly for 12 weeks, with open label extension for another 3 months
Intervention Type
Other
Intervention Name(s)
Placebo
Intervention Description
Patients randomized to this arm will receive one placebo pill once weekly.
Primary Outcome Measure Information:
Title
Effect of Vitamin D Supplementation on Albuminuria in CKD Patients as Assessed by Urine Albumin/Creatinine Measures.
Description
Urine albumin and creatinine were measured on spot urine specimens.
Time Frame
3 months
Secondary Outcome Measure Information:
Title
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.
Description
25(OH) vitamin D levels were measured using liquid chromatography.
Time Frame
3 months
Title
Effect of Vitamin D Supplementation on Mean Systolic Blood Pressure as Measured by Ambulatory Blood Pressure in CKD Patients as a Secondary Outcome.
Time Frame
3 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
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
Exclusion Criteria:
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Michal Melamed, MD, MHS
Organizational Affiliation
Albert Einstein College of Medicine
Official's Role
Principal Investigator
Facility Information:
Facility Name
Montefiore medical center
City
Bronx
State/Province
New York
ZIP/Postal Code
10467
Country
United States
12. IPD Sharing Statement
Learn more about this trial
The Effects of Vitamin D Repletion in Vitamin D Deficient Patients With Stage 3 and 4 Chronic Kidney Disease
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