Pharmacogenomics of the Variability in the In Vivo Response to Glucocorticoids
Completed · Phase 1
Conditions studied: Glucocorticoids Toxicity, Glucose Intolerance
In brief
This study evaluates the effect of acute administration of oral prednisone in white blood cells counts and glucose tolerance and the relationship of these measures with changes in gene expression in healthy volunteers. White blood cells counts, glucose tolerance and gene expression will be study before and after prednisone administration.
Key facts
- Study ID
- NCT03023891
- Run by
- Vanderbilt University Medical Center
- People needed
- 25
- Starts
- 2017-02-15
- Expected to finish
- 2019-12-31
- Last updated by the study team
- 2020-06-04
Who can join
Age: 18 and older, up to 45. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- 18 to 45 years old (to exclude the effect of age on glucose tolerance);
- BMI between 20 and 25 kg/m2 (to exclude individuals that are likely to have impaired insulin response);
- Normal fasting glucose;
- Stable weight for three months before participation
You may not qualify if…
- BMI >25kg/m2;
- Fasting glucose ≥126 mg/dl
- Shift work or disordered sleep (to exclude individuals with alterations in the hypothalamus-adrenergic axis);
- Any diseases;
- Use of any medication regularly (including over-the-counter);
- Previous exposure to glucocorticoids (within the last year);
- Pregnancy
Where it is running
- Vanderbilt University Medical Center -CRC — Nashville, Tennessee, United States
Full record on ClinicalTrials.gov
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