Vitamin D Deficiency in Chronic Kidney Disease (CKD) Patients

Completed · Phase 4

Conditions studied: Secondary Hyperparathyroidism, Chronic Kidney Disease

In brief

This is an open label, single center, randomized, active comparator controlled study, comparing the effects of vitamin D replacement using oral ergocalciferol versus paricalcitol on parathyroid hormone (PTH) levels in patients with stage 3 and 4 CKD and vitamin D deficiency or insufficiency. The purpose of this study is to determine which of these two approaches is more successful.

Key facts

Study ID

NCT00958451

Run by

Salem Veterans Affairs Medical Center

People needed

80

Starts

2009-07-01

Expected to finish

2011-01-01

Last updated by the study team

2011-03-24

Who can join

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

You may qualify if…

• Male or female chronic kidney disease patients at least 18 years of age.
• Patients should be able and willing to provide written informed consent and HIPAA Authorization.
• Chronic kidney disease stage 3 or 4.
• Plasma intactPTH level above 75pg/ml.
• Serum 25 OHD level below 30ng/ml.
• Negative pregnancy test unless 2 years postmenopausal or with a documented tubal ligation or total hysterectomy.
• Patients need to be off of any Vitamin analogues or preparations for 4 weeks prior to screening.

You may not qualify if…

• Women who are breast feeding, pregnant, capable of becoming pregnant, and not participating in an acceptable form of birth control.
• Patients currently participating in a clinical trial with another investigational drug or device or who have receive an investigational drug or device within 30 days of enrollment in this study.
• Major surgery within one month prior to enrollment or planned surgery while patient is in study (other than dialysis vascular access surgery).
• Patients who have had a malignancy unless they have received curative treatment and have been disease free for 2 years.
• Patients with a medical status that the PI decides would preclude participation.
• Patients on hemodialysis or peritoneal dialysis.
• Patients with a functional renal transplant.
• Patients with allergies to study drugs.
• Patients with acute renal failure with the past 12 weeks.
• Patients with clinically significant gastrointestinal or liver disease.
• Patients with active granulomatous disease.
• Patients with urine calcium:creatinine ratio of more than 0.2.
• Patients who received vitamin D analogs, calcimimetics, or biphosphonates within 4 weeks before screening. Treatment with any one of these medicines during the study is not permitted.

Where it is running

• VA Medical Center — Salem, Virginia, United States

Full record on ClinicalTrials.gov

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