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临床试验/NCT00688077
NCT00688077已完成不适用

Evaluation of FGF-23 Suppressibility by Calcitonin in Healthy Men - Pilot Study

Rijnstate Hospital1 个研究点 分布在 1 个国家目标入组 49 人开始时间: 2008年5月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
49
试验地点
1
主要终点
A change of 25% in de serum FGF-23 levels in response to a single subcutaneous injection of calcitonin 200 IU.

研究概览

简要总结

Introduction:

Based on our experience with calcitonin as an FGF-23 suppressive agent in a patient with an FGF-23 producing tumor we hypothesize that calcitonin may be a physiologically important regulator of FGF-23 production and secretion in healthy humans.

Aim:

In this study we wish to examine the FGF-23 suppressive effects of calcitonin in healthy men.

Study Design:

placebo-controlled, cross-over study

Method:

  • All twelve subjects are examined on two occasions, once after exposure to placebo 1 ml NaCl 0.9% subcutaneously, and once following calcitonin 200 IU/ml subcutaneously
  • On both occasions frequent bloodsampling will take place, out an indwelling catheter in de forearm vein.
  • Sampling times: -15, 0, 60, 120, 240, 360, and 480 minutes
  • Mealtimes: Calcium and Phosphate intake standardized on both occasions
  • All samples are analyzed for FGF-23, using a C-terminal FGF-23 ELISA kit (Immunotopics, San Clemente, USA) that measures intact and C-terminal fragments of FGF-23, and one that measures only intact FGF-23
  • Samples obtained at T-15, T0, T240 and T480 are stored for later analysis of Ca, albumin, PO4, PTH, 25-OHD and 1,25-OHD

Endpoint:

A change of 25% in de serum FGF-23 levels in response to a single subcutaneous injection of calcitonin 200 IU.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Crossover
主要目的
Basic Science
盲法
Single (Participant)

入排标准

年龄范围
20 Years 至 55 Years(Adult)
性别
Male
接受健康志愿者

入选标准

  • Healthy man, who are between 20-55 years old, and have a BMI 20-27 kg/m2.

排除标准

  • Serum creatinin >100 mmol/L, or glomerular filtration rate <80 ml/min.
  • Abnormal serum Ca, PO4, albumin, 25-OH vitamin D, or PTH levels.
  • Any medication.

研究组 & 干预措施

1

Experimental

干预措施: Calcitonin (Drug)

2

Placebo Comparator

NaCl 0,9% 2 ml, single subcutaneous injection

干预措施: Placebo (Drug)

结局指标

主要结局

A change of 25% in de serum FGF-23 levels in response to a single subcutaneous injection of calcitonin 200 IU.

时间窗: eight hours

次要结局

未报告次要终点

研究者

发起方
Rijnstate Hospital
申办方类型
Other

研究点 (1)

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