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Clinical Trial Summary

The purpose of this study is to compare infection rates when patients, elected for primary or aseptic revision THA / TKA, have a single intravenous antibiotic dose versus one single intravenous antibiotic dose in combination with intra-articular antibiotics. This is a prospective, randomized clinical survey on selected outcome measurements on 1834 subjects who will be recruited in a period of about 2 years.


Clinical Trial Description

Group A: patients receiving single dose of IV cefazolin 10-60 minutes before incision. Group B: patients receiving a single dose of IV cefazolin 10-60 minutes before incision + a single dose of intra-articular vancomycin powder before articulation (hip or knee) closure. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04399642
Study type Interventional
Source Centre Integre Universitaire de Sante et Services Sociaux du Nord de l'ile de Montreal
Contact Benoit Benoit, MD
Phone 514-338-2222
Email ben1000ben@icloud.com
Status Recruiting
Phase N/A
Start date July 5, 2019
Completion date December 31, 2027

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