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Clinical Trial Summary

This study is a multi-center open-label randomized study, and we sought to investigate the redundancy of post-procedural prophylactic antibiotics in cardiac implantable electronic device implantation. There are 2 arms in this study. One arm will receive pre-procedural intravenous antibiotics only. The other arm will receive both pre-procedural intravenous antibiotics and post-procedural 3-day oral antibiotics.


Clinical Trial Description

There is general agreement on the benefits of preoperative prophylactic antibiotics which had been documented in previous studies. Concerns of bacterial resistance and unnecessary cost, our prospective observational case-control study had suggested the redundancy of post-procedural antibiotics. In this well-designed study, we sought to investigate the efficacy of post-procedural antibiotics and confirm the hypothesis. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04146883
Study type Interventional
Source National Cheng-Kung University Hospital
Contact Hui-Chen Chiang, Bachelor
Phone +886-6-2353535
Email atiffany543783@gmail.com
Status Recruiting
Phase N/A
Start date August 20, 2019
Completion date December 31, 2021

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