Full Text View
Tabular View
No Study Results Posted
Related Studies
FGF-23 Suppressibility by Calcitonin
This study is currently recruiting participants.
Study NCT00688077   Information provided by Rijnstate Hospital
First Received: May 28, 2008   Last Updated: May 30, 2008   History of Changes

May 28, 2008
May 30, 2008
May 2008
September 2008   (final data collection date for primary outcome measure)
A change of 25% in de serum FGF-23 levels in response to a single subcutaneous injection of calcitonin 200 IU. [ Time Frame: eight hours ] [ Designated as safety issue: No ]
Same as current
Complete list of historical versions of study NCT00688077 on ClinicalTrials.gov Archive Site
 
 
 
FGF-23 Suppressibility by Calcitonin
Evaluation of FGF-23 Suppressibility by Calcitonin in Healthy Men - Pilot Study

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.

 
 
Interventional
Basic Science, Non-Randomized, Single Blind (Subject), Placebo Control, Crossover Assignment, Efficacy Study
Hypophosphatemia
  • Drug: Calcitonin
  • Drug: Placebo
Placebo Comparator: NaCl 0,9% 2 ml, single subcutaneous injection
 

*   Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.
 
Recruiting
12
 
September 2008   (final data collection date for primary outcome measure)

Inclusion Criteria:

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

Exclusion Criteria:

  • 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.
Male
20 Years to 55 Years
Yes
Contact: Hans Boer de, MD, PhD 31-2-6378-8888 hdeboer@alysis.nl
Contact: Carmen Horjus, MD chthorje@alysis.nl
Netherlands
 
NCT00688077
H. de Boer MD. PhD., Rijnstate Hospital, Arnhem
LTC-524/030408
Rijnstate Hospital
 
 
Rijnstate Hospital
May 2008

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP