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Completed

NCT Number: NCT00755690

Study of Dietary Phosphate and Mineral Homeostasis in Early Chronic Kidney Disease

This study is designed to describe the physiological response to increased and decreased dietary phosphate intake on various parameters of mineral metabolism in the blood and urine of individuals with Chronic Kidney Disease stage 3 and 4 with normal serum phosphate levels. This detailed study will give us a far greater understanding of the role of diet in abnormal mineral homeostasis early in the progression of this chronic disease. The findings of this study will help both physicians and dietitians better determine the optimal time to introduce dietary therapy in CKD.

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Key information

About this study

The potential benefits of implementation of phosphate management earlier in CKD (Stages 3/4) are threefold: 1) prevention of vascular damage early in the progression of CKD thus reducing risk of cardiovascular death 2) Improved management of renal bone disease and resultant co-morbidities and 3) slowing the progression of renal failure lengthening the time required till dialysis is required. Although dietary counseling is currently a normal part of CKD care, the utility and effectiveness of lowering phosphate has not previously been quantified. In part this is due to the difficulty of measurement of serum phosphate as it is so tightly controlled before GFR falls below 30mls/min. No studies have investigated whether is it possible to modulate circulating FGF-23 and phosphate excretion in early stages of renal failure using diet in individuals with normal serum phosphate levels.

Study Objectives ;

  • To measure FGF-23 levels before and after a high phosphate diet, low phosphate diet and a low phosphate diet with phosphate binders.
  • To measure levels of calcium, phosphate, PTH, 25 and 1,25 vitamin D and fractional phosphate excretion before and after a high phosphate diet, low phosphate diet and a low phosphate diet with phosphate binders.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • CKD patients with CKD stage 3 and 4 (eGFR < 60 ml/min and > 15 ml/min per 1.73 m2, not requiring dialysis).
  • Normal serum phosphate stable over three months (> 0.87 mmol/L and < 1.70 mmol/L)
  • Not yet following a low phosphate diet as reported by the patient or the renal dietitian (<1500mg/d)
  • Over 19 years of age

Exclusion criteria

  • Body mass index <20 kg/m2
  • Current use of phosphate binders or active vitamin D or phenytonin (which induces vitamin D catabolism)
  • Primary parathyroid defects
  • Diagnosed osteoporosis
  • Gut absorption defects
  • Liver disease
  • Pregnancy or lactation
  • Patients hospitalised within the last 4 weeks

Treatment and study plan

High/ Low Phosphate diet

Behavioral

Low phosphate diet (750mg/day).

Primary outcomes

  1. FGF-23

    Time frame: 5 days

Secondary outcomes

  1. Serum calcium, phosphate, PTH, 25 and 1,25 vitamin D and fractional phosphate excretion.

    Time frame: 5 days

Sponsors and collaborators

Lead sponsor

University of British Columbia

Other

Registry information

Important dates

Study start
2008
Primary completion
2010
Study completion
2010
First posted
Sep 19, 2008
Registry last updated
Feb 19, 2014

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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