Simi Valley, California 93063


Purpose:

The purpose of the study is to determine whether an ingestion of a new renal multivitamin supplement can have a beneficial effect on bone and mineral adn inflammation issues related to patients on dialysis.


Criteria:

Inclusion Criteria: - End stage renal disease patients on dialysis for at least 90 days deemed to be at low risk by the investigator for being hospitalized or have concurrent infections - Serum phosphorous level > 5 mg/dl - Stable phosphate binder regimen for 2 week prior to enrollment - Stable dose of Vitamin D for 4 weeks prior to enrollment - Stable calcimimetic dose for 4 week prior to enrollment Exclusion Criteria: - patients who are pregnant - patients who have pre existing thrombocytopenia defined as a platelet count of <100 x 109/L - abnormal LFTs - baseline CRP > 15 g/dl - known sensitivity to any of the active ingredients - patients who are currently enrolled in a clinical trial, or who have been in a clinical trial in the last six months - are currently taking any immunosuppressive medications


NCT ID:

NCT00834301


Primary Contact:

Study Director
Ray Chow, PhD
Nephrian


Backup Contact:

N/A


Location Contact:

Simi Valley, California 93063
United States

Kant Tucker, MD
Phone: 805-433-7500

Site Status: Recruiting


Data Source: ClinicalTrials.gov

Date Processed: October 09, 2019

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