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Clinical Trial Summary

Ofloxacin is a gold standard antibiotic for the treatment of bone and joint infections due to sensible staphylococcus strains. However, in the elderly, inter-individual variability of the pharmacokinetics may reduce the efficacy or increase toxicity. The occurrence of ofloxacin side effects is likely to be increased in case of higher exposition. However, the serum concentration-toxicity relationship has not yet been determined. The purpose of this project is to assess the association between the residual serum concentration of ofloxacin at day 3 and the occurrence of at least one adverse effect attributable to ofloxacin, and determine a threshold toxicity concentration if this association exists.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04496024
Study type Interventional
Source Centre Hospitalier Universitaire, Amiens
Contact Youssef BENNIS, MD
Phone (33)32208700
Email bennis.youssef@chu-amiens.fr
Status Recruiting
Phase N/A
Start date June 2, 2020
Completion date August 2023

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