Clinical Trials Directory

Trials / Completed

CompletedNCT03388203

LC-MS/MS 25(OH)D Status in a Large Cohort

LC-MS/MS Based 25(OH)D Status in a Large Central European Outpatient Cohort- Gender and Age Specific Differences

Status
Completed
Phase
Study type
Observational
Enrollment
74,235 (actual)
Sponsor
Azienda Ospedaliera di Bolzano · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The present study assessed serum 25(OH)D in a cohort of 74235 outpatients by liquid-chromatography-tandem-mass-spectrometry (LC-MS/MS). The investigators studied the distribution of serum 25(OH)D concentrations in males and females of different age groups, the prevalence of measurable amounts of 25(OH)D2 and seasonal variability.

Detailed description

Measurements were performed under routine circumstances. Samples were collected in serum tubes with clot-activator. As per routine procedure, samples were centrifuged upon arrival in the lab and stored at 4° C until measurement. 25(OH)D3 and 25(OH)D2 were quantitated separately. Results from subjects \<18 years were excluded from the analysis. The study was approved by the local Ethics Committee.

Conditions

Interventions

TypeNameDescription
DIAGNOSTIC_TEST25(OH)D measurement, PTH measurement25(OH)D analyses by LC-MS/MS were performed as part of our routine clinical work with a commercial kit from Recipe (Munich, Germany) ; PTH was measured in lithium-heparin plasma using the PTH STAT assay from Roche Diagnostics (Mannheim, Germany) on a Cobas 8000 auto-analyzer.

Timeline

Start date
2015-01-01
Primary completion
2016-12-01
Completion
2017-06-01
First posted
2018-01-02
Last updated
2018-01-02

Source: ClinicalTrials.gov record NCT03388203. Inclusion in this directory is not an endorsement.