drugset / Trial / NCT03247920

Reduction of Intravenous Antibiotics In Neonates

NCT03247920

Phase 4 Completed 510 enrolled Franciscus Gasthuis Erasmus Medical Center · collab
RandomizedParallel-groupSingle-blindTreatment

Summary

Randomized controlled open-label non-inferiority trial comparing complete intravenous antibiotic treatment with a short iv. course followed by oral antibiotics in neonates (0-28 days) with probable bacterial infection. Primary outcome: \- Bacterial re-infection within 28 days after finishing of antibacterial therapy. Secondary outcome(s): * Pharmacokinetic profile of oral amoxicillin/clavulanic acid * Quality of life * Cost-effectiveness * Alterations in gut microbiome * Use of molecular techniques for better detection of bacterial pathogens

Timeline

Start
2017-11-04
Primary completion
2021-06-15
Completion
2021-07-15

Drugs

EvaluationDrugModalityDoseRoute
Comparator Amoxicillin Other / unclassified 75 mg/kg Oral
Comparator clavulanic acid Small molecule 18.75 mg/kg Oral

Indications