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Completed

NCT Number: NCT00889629

Pilot Study Evaluating Doxercalciferol Replacement Therapy in Kidney Transplant Recipients

People with kidney transplants often develop bone disease. One reason for bone disease may be overactivity of a gland in the neck called the parathyroid gland. Overactivity of the parathyroid gland may be caused by lack of Vitamin D in the body. It has recently been discovered that many patients with kidney transplants have low Vitamin D levels. The investigators are examining the effects of doxercalciferol on parathyroid hormone levels, proteinuria and bone turnover markers in people who have had a kidney transplant.

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Key information

About this study

People with kidney transplants often develop bone disease. One reason for bone disease may be overactivity of a gland in the neck called the parathyroid gland. Overactivity of the parathyroid gland may be caused by lack of Vitamin D in the body. It has recently been discovered that many patients with kidney transplants have low Vitamin D levels.

25-OH Vitamin D3 is now recommended to treat kidney transplant patients with low vitamin D levels but it may not be enough to treat the parathyroid problems and bone disease. Doxercalciferol is a form of Vitamin D that has been used to treat bone disease and parathyroid problems in dialysis patients but has not yet been studied in patients with kidney transplants. We are interested in seeing whether doxercalciferol given together with 25-OH Vitamin D3 will be a better treatment for the overactive parathyroid gland and bone disease than 25-OH Vitamin D3 alone in patients with kidney transplants.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Adults of both genders between the ages of 18 and 65.
  • Kidney transplant at least 1 year prior to enrollment
  • Creatinine value of <2.5 mg/dl with no excursion >0.5 within the past 3 months
  • Proteinuria of 500 mg/24 hours or a protein/creatinine ratio of 0.5 or greater
  • Hypovitaminosis D, as defined by a 25-OH Vitamin D value of <25 ng/ml
  • Intact PTH value between 150 and 600 pg/ml

Exclusion criteria

  • History of parathyroidectomy
  • History of prior intolerance to vitamin D therapy (not including hypercalcemia)
  • History of biopsy proven acute rejection over the 3 months preceding enrollment
  • Recent (over the past month) addition of an ACE inhibitor or Angiotensin -
  • Receptor Blocking agent - patients who have been on a stable dose are acceptable
  • Current use of active Vitamin D supplement (patients in whom therapy has been discontinued more than 1 month prior to enrollment are acceptable)
  • Postmenopausal woman or women receiving hormone replacement therapy

Treatment and study plan

Doxercalciferol

Drug

Active group receives doxercalciferol (Hectorol) 1mcg

Other names: Hectorol (the other name for Doxercalciferol)

Placebo

Drug

Group 2 receives placebo (dummy bottle with pills resembling doxercalciferol)

Other names: Placebo for doxercalciferol

25-OH Vitamin D3

Drug

All groups received cholecalciferol

Other names: (cholecalciferol)

Primary outcomes

  1. - iPTH value of 100 pg/ml or lower

    Time frame: 6 months

    The number of patients achieving the target iPTH value of 100 pg/ml or lower measured. Change in the level of iPTH (baseline as compared with 3 and 6 months) using both absolute value and percent change from baseline.

Secondary outcomes

  1. Change in 1,25 D2 and D3, 25-OH Vitamin D3 levels

    Time frame: 6 months

    The Change in the levels of 1,25 D2 and D3, 25-OH Vitamin D3 levels (baseline as compared with 3 month and end of study)

  2. Change in FGF-23 levels

    Time frame: 6 months

    The Change in FGF-23 levels (baseline as compared with 3 and 6 months) were measured.

  3. Change in serum bone turnover markers

    Time frame: 6 months

    The Change in the levels of serum osteocalcin, bone alkaline phosphatase and n-telopeptide of Type I collagen levels (baseline versus 3 and 6 months

  4. Change in Protein/creatinine ratio

    Time frame: 6 months

    Change in the level of Protein/creatinine ratio and or 24 hour urine for protein (baseline as compared with 3 and 6 months)

    • Change in the level of Protein/creatinine ratio (baseline as compared with 3 and 6 months)

    The Change in the level of Protein/creatinine ratio (baseline as compared with 3 and 6 months)

Sponsors and collaborators

Lead sponsor

Mariana Markell

Other

Collaborators

  • Genzyme, a Sanofi Company

Registry information

Official study title

Pilot Study: Effects of Hectorol (Doxercalciferol) Vitamin D Replacement on Proteinuria, PTH Level and Bone Turnover in Stable Kidney Transplant Recipients: a Single-Blind, Placebo-Controlled Study in Patients Receiving 25-OH Vitamin D3

Important dates

Study start
2008
Primary completion
2010
Study completion
2010
First posted
Apr 29, 2009
Registry last updated
Feb 22, 2019

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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