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RECRUITING NA

Vancomycin Reduction Practices (VRP) in the NICU

NCT06772675 · View on ClinicalTrials.gov ↗

Study 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.

Interventions

  • BEHAVIORAL External Facilitation

Study Locations (13)

California

  • Kaiser Permanente Modesto Medical Center — Modesto
  • Kaiser Permanente East Bay - Oakland Medical Center — Oakland
  • Kaiser Permanente Roseville Medical Center — Roseville
  • Kaiser Permanente San Francisco Medical Center — San Francisco
  • Kaiser Permanente San Leandro Medical Center — San Leandro
  • Kaiser Permanente Santa Clara Medical Center — Santa Clara
  • Kaiser Permanente Walnut Creek Medical Center — Walnut Creek

Pennsylvania

  • Lancaster General Hospital — Lancaster
  • Hospital of the University of Pennsylvania — Philadelphia
  • Pennsylvania Hospital — Philadelphia
  • Chester County Hospital — West Chester

New Jersey

  • Medical Center of Princeton — Plainsboro
  • Virtua Voorhees — Voorhees Township

Trial Details

FieldValue
Enrollment Target 13 participants
Start Date 2025-06-02
Est. Completion 2027-09
Phase NA

Sponsor

Children's Hospital of Philadelphia

492 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06772675

The ClinicalTrials.gov registry entry for NCT06772675 describes a study currently listed as recruiting. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 13 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Children's Hospital of Philadelphia, which has 492 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 3 conditions, with Antibiotic Stewardship appearing as the primary indexed condition, and to 1 intervention — of which External Facilitation is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT06772675 reports 13 study locations spanning 3 distinct geographic areas — top geographies include California, Pennsylvania, New Jersey. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT06772675 about?

NCT06772675 is a clinical study titled "Vancomycin Reduction Practices (VRP) in the NICU". 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-lev...

What is the current status of trial NCT06772675?

This trial is currently recruiting. It is a NA study. The enrollment target is 13 participants. The study started on 2025-06-02. Estimated completion is 2027-09.

What conditions does trial NCT06772675 study?

This clinical trial studies the following conditions: Antibiotic Stewardship, Neonatal Sepsis, Late-Onset, Vancomycin. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT06772675?

The interventions under investigation include: External Facilitation (BEHAVIORAL). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT06772675?

This trial is sponsored by Children's Hospital of Philadelphia, which has 492 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT06772675 being conducted?

This trial has 13 study locations across California, New Jersey, Pennsylvania. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial