Loading
Life sciences · Interventional Study
ClinicalTrials.gov · September 24, 2026
No summary has been generated for this record yet. What follows is drawn from its source metadata only.
Interventional Study.
No findings were extractable from the material analysed.
Safety was not reported in the material analysed. Check the source before drawing any conclusion about harm.
The source did not state who this applies to in practice.
Graded across the dimensions that decide whether you should act, each from what the source actually supports. There is no single score, and where a dimension was not assessed it says so.
This record has not been graded across any dimension yet. Treat the label above as provisional and read the source.
What is missing. This record has no bottom line, key findings, reported figures, evidence dimensions. That is a gap in the analysis, not a judgement about the study.
Registry record from ClinicalTrials.gov (NCT06772675). This is a study registration, not published results. Lead sponsor: Children's Hospital of Philadelphia. Recruitment status: RECRUITING. Phase: NA. Study type: INTERVENTIONAL. Enrollment: 13 participants (ESTIMATED). Conditions: Antibiotic Stewardship, Neonatal Sepsis, Late-Onset, Vancomycin. Interventions: BEHAVIORAL: External Facilitation. Primary outcome measures: Fidelity of VRP use , 2.5 years - From beginning of implementation phase to the end of the sustainment phase. Brief summary: This multi-center, cluster randomized study aimed at improving implementation of vancomycin reducing practices (VRP) in neonatal intensive care units (NICUs). Sites will be recruited and randomized to receive either external facilitation or no external facilitation to assess the effect on center-level fidelity to the core components of VRP implementation. Interventions available to both study arms are directed at hospital staff and includes identification of local champions, educational outreach, unit-level audit \& feedback, and use of a clinical decision support tool.