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Efficacy of seven and fourteen days of antibiotic treatment in uncomplicated Staphylococcus aureus bacteremia: A randomized, non-blinded, non-inferiority interventional study

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2024-519186-21-01
Enrollment
264
Registered
2025-01-30
Start date
2025-01-30
Completion date
Unknown
Last updated
2025-11-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Staphylococcus aureus bacteremia

Brief summary

90-day survival without clinical or microbiological failure to treatment or relapse in patients treated with 7 days versus 14 days of antibiotic therapy

Detailed description

All-cause mortality days 14, 28, 90 and 180, Microbiological failure to treatment, Microbiological relapse, Clinical failure to treatment, Severe adverse events grade ≥3, Severe adverse events grade ≥3, Clostridium difficile infection, Multidrug-resistance organism, Health-associated costs associated the treatment lengths, Desirability of outcome ranking (DOOR), Hospital admissions during follow up

Interventions

DRUGBenzylpenicillin ”Panpharma”
DRUGopløsning
DRUGClarithromycin ”Alternova”
DRUGCefuroxim Fresenius Kabi
DRUGPrimcillin
DRUGfilmovertrukne tabletter 800 mg
DRUGGentamicin ”B. Braun”
DRUGBactocin
DRUGClarithromycin "Accord"
DRUGFlucloxacillin ”Orion”
DRUGCloxacillin "Stragen"
DRUGpulver til injektions-/infusionsvæske
DRUGClindamycin "Abcur"
DRUGDicloxacillin "Alternova"
DRUGPiperacillin/Tazobactam "Sandoz"
DRUGDaptomycin "Accord Healthcare"
DRUGCeftriaxon "Kalceks"
DRUGfilmovertrukne tabletter 400 mg
DRUGAmikacin "Macure"
DRUGinjektionsvæske
DRUGLinezolid Fresenius Kabi
DRUGCefotaxim "MIP"
DRUGMoxifloxacin "Accord"
DRUGPiperacillin/Tazobactam ”Sandoz”
DRUGMeropenem Fresenius Kabi
DRUGMoxifloxacin Fresenius Kabi
DRUGFlucloxacillin "Orion"
DRUGLevofloxacin "Macure"
DRUGLinezolid "Teva"

Sponsors

Hvidovre Hospital
Lead SponsorOTHER

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Design outcomes

Primary

MeasureTime frame
90-day survival without clinical or microbiological failure to treatment or relapse in patients treated with 7 days versus 14 days of antibiotic therapy

Secondary

MeasureTime frame
All-cause mortality days 14, 28, 90 and 180, Microbiological failure to treatment, Microbiological relapse, Clinical failure to treatment, Severe adverse events grade ≥3, Severe adverse events grade ≥3, Clostridium difficile infection, Multidrug-resistance organism, Health-associated costs associated the treatment lengths, Desirability of outcome ranking (DOOR), Hospital admissions during follow up

Countries

Denmark

Outcome results

None listed

Source: EU CTIS · Data processed: Feb 4, 2026