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Serum FGF-23 and Vitamin D Deficiency

I

Istanbul University

Status

Completed

Conditions

Osteomalacia

Study type

Observational

Funder types

Other

Identifiers

NCT01102751
Research Fund (Other Identifier)
Istanbul University

Details and patient eligibility

About

We aimed to determine the effect of vitamin D replacement therapy on serum FGF-23 concentrations in vitamin D deficient women and to compare the FGF-23 concentrations of vitamin D deficient patients with healthy subjects and patients with genetically-determined hypophosphatemic rickets.

Full description

Study group was composed of vitamin D deficient females (n =18, mean age 29.1±9.9 yrs), vitamin D sufficient healthy females (control group; n = 19, mean age 28.5±5.2 yrs) and patients with genetically-determined hypophosphatemic rickets (n=13, mean age 26.5±15.1 yrs). Groups were compared for serum FGF-23, 1,25 dihydroxy vitamin D3, calcium, phosphate, bone turnover markers, intact parathyroid hormone and urinary excretion of calcium and phosphate. Vitamin D deficient group was re-evaluated after a standard treatment regimen.

Sex

All

Ages

9 to 44 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Serum 25OHD Vitamin <30 ng/mL for group 1
  • Serum 25OHD Vitamin >30 ng/mL for control group

Exclusion criteria

  • Receiving medication(s) affecting bone metabolism
  • History of gastrointestinal disease and malabsorption
  • History of renal and liver disease

Trial design

0 participants in 3 patient groups

Vitamin D deficient females
Description:
(n =18, mean age 29.1±9.9 yrs)
vitamin D sufficient healthy females
Description:
(control group; n = 19, mean age 28.5±5.2 yrs)
genetically-determined hypophosphatemic rahitis
Description:
(n=13, mean age 26.5±15.1 yrs)

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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