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Completed

NCT Number: NCT00438932

Low Phosphate Diets in Patients With Early Stages of Chronic Kidney Disease

The purpose of this study is to learn more about how the kidneys control the blood levels of phosphorus in patients with early chronic kidney disease. The ultimate goal is to use this information to design improved treatment strategies for phosphorus-related problems for the millions of patients with chronic kidney disease.

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Key information

Age range

18 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Massachusetts General Hospital

Boston, Massachusetts, 02114, United States

About this study

Phosphorus is a mineral found in dairy products, nuts, and meat that is essential for bone health and many other important functions inside the body's cells. The kidneys are responsible for keeping the blood levels of phosphorus normal. Healthy kidneys do this by spilling excess phosphorus into the urine. In patients with chronic kidney disease, the kidneys are unable to spill an adequate amount of phosphorus so that excess phosphorus can accumulate in the walls of blood vessels leading to heart disease, their leading cause of death. A recently discovered hormone called FGF-23 helps control the blood levels of phosphorus by "telling" the kidney how much phosphorus to spill in the urine. The purpose of this study is to learn more about how FGF-23 helps the kidneys control the blood levels of phosphorus. The ultimate goal is to use this information to design improved treatment strategies for phosphorus-related problems for the millions of patients with chronic kidney disease.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • subjects with stage 3a, 3b and 4 CKD
  • subjects have to be aged 18 years or older
  • subjects have to have normal serum phosphate levels (< 4.6 mg/dl)
  • subjects have to have sufficient 25-OH Vit0amin D levels (≥ 20 ng/ml)

Exclusion criteria

  • subjects with rapidly advancing renal failure who thus might develop hyperphosphatemia or end stage renal disease requiring initiation of dialysis during the study period
  • subjects expected to require dialysis initiation within the follow up period
  • subjects with hyperphosphatemia > 4.6 mg/dL
  • subjects with any previous or current treatment with phosphate binders or active vitamin D (doxercalciferol or calcitriol)
  • subjects with malnutrition, defined as a serum albumin < 3.0 mg/dl, in order to avoid worsening protein-malnutrition status during the restricted study period since phosphate restricted diets are also low in protein
  • subjects with chronic gastrointestinal diseases that could impede their absorptive ability such as Crohn's disease, ulcerative colitis and sprue
  • subjects with liver disease (ALT or AST > 100 U/L) or cholestasis (direct bilirubin > 1.0 mg/dl) because this can limit their ability to absorb fat soluble vitamins such as vitamin D
  • subjects with anemia, defined as a hematocrit <27% at the screening visit
  • subjects wht have been hospitalization within the previous 4 weeks
  • subjects who are pregnant
  • subjects who are breastfeeding mothers
  • subjects with primary hypoparathyroidism
  • subjects with primary hyperparathyroidism
  • subjects with previous subtotal parathyroidectomy
  • subjects with previous outpatient counseling by a renal nutritionist
  • subjects who are unable to independently provide written informed consent - prisoners, mentally incompetent, minors

Treatment and study plan

Lanthanum carbonate

Drug

Lanthanum carbonate 1000mg 3x/day

Low Phosphorus Diet

Dietary Supplement

Low phosphorus diet will consist of 800 mg of phosphorus per day.

Unrestricted Phosphorus Diet

Dietary Supplement

Unrestricted diet will contain 1550 mg of phosphorus per day - 800 mg of which is dietary and 750mg of Neutraphos (3 packets/day); each packet is 250mg.

Other names: Neutraphos

Placebo

Drug

Lanthanum Carbonate placebo given three times a day with meals.

Primary outcomes

  1. Fibroblast Growth Factor 23 (FGF-23)

    Time frame: 2 weeks

    Plasma FGF-23 was measured using c-terminal FGF23 assay.

Secondary outcomes

  1. 24-hour Urinary Phosphate

    Time frame: 2 weeks

    from 24-hr urine collections

Sponsors and collaborators

Lead sponsor

Massachusetts General Hospital

Other

Collaborators

  • Shire

Registry information

Official study title

Reduced Phosphate Intake in "Normo-Phosphatemic" Chronic Kidney Disease Patients

Important dates

Study start
2007
Primary completion
2010
Study completion
2010
First posted
Feb 22, 2007
Registry last updated
Sep 27, 2011

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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