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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01835639
Other study ID # 12-009753
Secondary ID K23DK093556
Status Completed
Phase N/A
First received
Last updated
Start date April 2013
Est. completion date September 2017

Study information

Verified date August 2019
Source Children's Hospital of Philadelphia
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This multi-site, pilot study will assess vitamin D supplementation in children and young adults with Glomerular Disease. .


Description:

Vitamin D deficiency has been linked to a variety of adverse health outcomes. Nephrotic patients have very low vitamin D levels, and the underlying mechanisms are not known. Furthermore, approaches to safely and effectively supplement vitamin D in these patients have not been established. The purpose of this research study is to learn if vitamin D supplementation is safe and effective in patients with primary glomerular disease and to also help establish the treatment guidelines. About 35 patients with primary glomerular disease, ages 5-30 years old, will take part in this study. Participants will be asked to take vitamin D supplements each day for 12 weeks and will have 3 study visits.


Recruitment information / eligibility

Status Completed
Enrollment 32
Est. completion date September 2017
Est. primary completion date September 2017
Accepts healthy volunteers No
Gender All
Age group 5 Years to 30 Years
Eligibility Inclusion Criteria:

- Males or females, age 5-30 years

- Diagnosis of primary glomerular disease (such as steroid-resistant nephrotic syndrome, minimal change disease, FSGS, membranous nephropathy, membranoprolfierative glomerulonephritis, and Immunoglobulin A [IgA] nephropathy) without systemic inflammatory disorders (i.e. lupus, vasculitis)

- Serum 25(OH)D level <30 ng/ml and urine protein:creatinine ratio =0.5 at Screening Visit.

Exclusion Criteria:

- Pregnancy

- estimated Glomerular Filtration Rate (eGFR) <30 ml/min/1.73m2 at Screening Visit

- Serum phosphorus > 5.5 mg/dl or hypercalcemia

- Chronic medical conditions or medications unrelated to the renal disease that may impact vitamin D status

- Known history of kidney stone(s)

Study Design


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
Cholecalciferol, 2000 or 4000 IUs by mouth daily for 12 weeks
Supplements will be provided as oral capsules.

Locations

Country Name City State
United States Johns Hopkins University,Division of Pediatric Nephrology Baltimore Maryland
United States North Shore-Long Island Jewish Health System New Hyde Park New York
United States Children's Hospital of Philadelphia Philadelphia Pennsylvania
United States The Hospital of the University of Pennsylvania Philadelphia Pennsylvania
United States Nemours/Alfred I. duPont Hospital for Children Wilmington Delaware

Sponsors (4)

Lead Sponsor Collaborator
Children's Hospital of Philadelphia American Society of Nephrology, National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK), The NephCure Foundation

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary To assess the efficacy of vitamin D supplementation, by the increase in total and free 25(OH)D levels. 12 weeks
Primary To assess the safety of vitamin D supplementation, by serum Ionized calcium (ICal), Pi, and 25(OH)D, and urinary calcium excretion. 12 weeks
Secondary To assess the innate immune response, measured by changes in the induction of Human cathelicidin antimicrobial protein (hCAP) in human monocytes. 12 weeks
Secondary To assess intra-renal inflammation, measured by changes in urinary Macrophage chemo-attractant protein 1 (MCP-1). 12 weeks
Secondary To assess arterial stiffness, measured by changes in pulse wave velocity. 12 weeks
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