Trial to Optimize Mineral Outcomes in Dialysis Patients

Completed · Phase 4

Conditions studied: Secondary Hyperparathyroidism, Chronic Kidney Disease

In brief

This trial is designed to determine if the use of a computer algorithm designed to optimize mineral outcomes in dialysis patients increases the number of patients achieving the desired target endpoints for calcium, phosphorus and parathyroid hormone.

Key facts

Study ID

NCT01100723

Run by

University of Colorado, Denver

People needed

92

Starts

2010-03-01

Expected to finish

2011-08-01

Last updated by the study team

2017-01-02

Who can join

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

You may qualify if…

• Men or women 18 years of age or older
• On outpatient hemodialysis
• Have a level of understanding and willingness to cooperate with the study personnel
• Able to provide informed consent

You may not qualify if…

• Currently enrolled in another interventional clinical trial
• Are pregnant, plan on becoming pregnant during the study period, or breast-feeding
• Planned parathyroidectomy within 6 months
• Planned kidney transplant within 6 months
• Life expectancy < 6 months
• Patient declines participation
• Liver function tests > 2 times the upper limit of normal

Where it is running

• Lynchburg Nephrology Associates, P.L.L.C. — Lynchburg, Virginia, United States

Full record on ClinicalTrials.gov

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