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Evidence Based QUality Improvement for Prescribing Stewardship in ICU (EQUIPS-ICU)

Study acronym: EQUIPS-ICU
StatusRecruiting
PhaseNot specified
Started
View on ClinicalTrials.gov ↗
Trial flagged as At Risk
Primary completion moved at least 1 year 7 months later May 2025 → Dec 31, 2026
See other at-risk trials from University of Oxford

Record History

See every version on ClinicalTrials.gov ↗

  1. Primary completion pushed from May 2025 to Dec 31, 2026 Show 7 more changesShow less
    • Recruitment opened
    • Study completion pushed from Sep 2025 to Dec 31, 2026
    • Study sites: 0 to 1
    • Start date changed from estimate of Nov 2024 to Jan 13, 2025
    • Secondary endpoints: details revised at 5 of 5 entries
    • Publications: details revised at 1 of 1 entry
    • Eligibility criteria expanded, about 3 words
  2. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
The goal of this observational study is to learn about the implementation of a process to review antimicrobial prescriptions for adult patients in Intensive Care Unit (ICU). The main question it aims to answer is: can a structured antimicrobial review can be implemented in ICUs? Implementation will be supported by the use of local protocols, audit and feedback, and education. It will be evaluated by daily data collection of clinical processes and interviews with local champions. Resources to conduct the study are provided by the Wellcome Flagship Innovations award. ("Collaboration for Research, Implementation and Training in Critical Care in Asia and Africa", reference 224048/Z/21/Z).
Trial Details
NCT Number NCT06666738
Lead Sponsor University of Oxford
Collaborators: Nat Intensive Care Surveillence-MORU
Conditions
(from sponsor)		 Antimicrobial Stewardship
Enrollment 6,300 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov