Identification of Markers for Determining the Efficacy of Vitamin D Receptor Activator Therapy in Stage 3/4 CKD Patients

Completed · Has a placebo group

Conditions studied: CKD Stage 3/4

In brief

The purpose of this study is to identify genes that are responsive to paricalcitol (active vitamin D) therapy. Scientists have found that over 30 different types of cells in the body respond to vitamin D therapy, including blood vessels. Low levels of vitamin D may reduce the amount of calcium in the blood, increase the amount of parathyroid hormone (PTH) and cause the parathyroid gland (small gland located in the neck) to get bigger which is called secondary hyperparathyroidism (SHPT). Also, low levels of vitamin D may worsen the heart disease seen in dialysis patients. Paricalcitol, a man-made active vitamin D, is a replacement for vitamin D for preventing and treating SHPT. Studies that followed patients on dialysis have found: (1) differences in death rates between those who received active vitamin D compared with no activated vitamin D, and (2) a survival benefit in chronic kidney disease (CKD) patients receiving paricalcitol, over calcitriol (natural active vitamin D). Researchers have considered that giving paricalcitol to people with (CKD) may also prevent or slow the progression of heart disease. Currently, physicians can only tell how well the vitamin D is working by measuring PTH concentrations. This study aims to identify markers in the blood that can be used to determine the efficacy of Vitamin D therapy.

Key facts

Study ID

NCT02018133

Run by

University of Illinois at Chicago

People needed

8

Starts

2009-12-01

Expected to finish

2012-06-01

Last updated by the study team

2020-08-17

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Chronic kidney disease stage 3/4
• PTH: >70 pg/ml
• If on ACEI/ARB, optimized and stable dose

You may not qualify if…

• Failure to provide informed consent
• Prior active vitamin D oral or parenteral treatment, including calcitriol, paricalcitol and doxercalciferol
• Glomerulonephritis requiring active treatment with immunosuppressive therapy
• Serum phosphorus: > 5.2 mg/dL
• Serum calcium (corrected for albumin): > 10.0 mg/dL
• Clinical unstable medical conditions (other than CKD)
• Use of any investigational drug within the past 30 days or 5 half-lives, whichever is longer
• History of malignancy, other than basal cell carcinoma of the skin
• History of hypersensitivity to vitamin D or its analogs
• Pregnant or nursing (lactating) women
• Women of child-bearing potential

Where it is running

• University of Illinois at Chicago — Chicago, Illinois, United States

Full record on ClinicalTrials.gov

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