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临床试验/ACTRN12609000250235
ACTRN12609000250235已完成4 期

Calcium citrate and its effects on bone loss and hyperparathyroidism in renal transplant recipients

Dr Patrick T Coates0 个研究点目标入组 35 人开始时间: 2009年5月12日最近更新:
适应症

试验速览

阶段
4 期
状态
已完成
发起方
入组人数
35

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Non-randomised trial
主要目的
Treatment
盲法
Open (masking not used)

入排标准

年龄范围
o limit 至 o limit(—)
性别
All

入选标准

  • Previous renal transplant over 1 year ago.
  • Stable renal function (Creatinine < 150) Standard immunosuppression regime (Tacrolimus, Mycophenolate Mofetil and Prednisolone).
  • Able to give informed consent.
  • Able to attend 3 sessions held over 1 week.

排除标准

  • Preexisting hypercalcemia (Ca > 2.55 mmol/L), severe hyperparathyroidism (PTH > 50 pmol/L) or severe vitamin D insufficiency (serum 25-hydoxy vitamin D < 15 ng/mL).
  • Previous parathyroidectomy.
  • Concurrent use of bisphosphonates, Vitamin D analogues, lithium, phenytoin, carbamazepine, hormone replacement therapy, thiazide diuretics.
  • Participation in a concurrent study.
  • Pre-menopausal women (due to low level radiation exposure).

研究者

发起方
Dr Patrick T Coates

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