About this trial
This study aims to provide high-level evidence for appropriate empirical antibiotic use tailored to the clinical reality in Korea by conducting a randomized controlled trial comparing monotherapy with piperacillin/tazobactam and combination therapy with piperacillin/tazobactam plus a fluoroquinolone in patients with severe community-acquired pneumonia.
Eligibility criteria
Qualifiers
Adult patients aged 19 years or older who visited the emergency department and were hospitalized.
Radiologic evidence of pulmonary infiltration on chest X-ray or chest CT.
Disqualifiers
Transferred from another hospital after >48 hours of hospitalization
Died within 72 hours of hospital admission
Transferred to another hospital within 14 days of admission
Pneumonia occurring after >48 hours of mechanical ventilation, including home ventilators
Trial design
Treatments tested in this trial
- Piperacillin/Tazobactam
- Piperacillin/tazobactam + Levofloxacin
Treatment groups
Sponsors and collaborators
CHOSEOK YOON
Lead sponsor
Seoul Hospital
Sponsor institution