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Mechanical Ventilation in Surgical Patients

Study acronym: MEET VENUS
StatusRecruiting
PhaseNot specified
Started
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Record History

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  1. Trial status: Not Yet Recruiting to Recruitingv4 Show 4 more changesShow less
    • Primary completion date: Sep 30, 2026 to Aug 31, 2027
    • Start date changed from estimate of Sep 1, 2025 to Mar 1, 2026
    • Study sites: 0 to 1
    • Study completion date: Mar 1, 2027 to Aug 31, 2027
  2. Lead sponsor: Azienda Ospedaliero Universitaria Maggiore della Carita to Azienda Ospedaliera SS. Antonio e Biagio e Cesare Arrigo di Alessandria
    • Primary completion date: Oct 31, 2024 to Sep 30, 2026
    • Start date: Jun 1, 2024 to Sep 1, 2025
    • Study completion date: Mar 31, 2025 to Mar 1, 2027
    v3
  3. Collaborators: 4 to 5v2
  4. 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  • Stopped: an ongoing trial was terminated, suspended or withdrawn.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.
This is an investigator-initiated, international, multicenter, prospective, cross-sectional study that aims to 1) describe the incidence and types of postoperative pulmonary complications (PPCs), 2) describe patient demographics, baseline characteristics, and intraoperative ventilation management, 3) describe the occurrence of intraoperative adverse events (IAEs), and 4) their associations with PPCs, 5) assess the practice of intraoperative mechanical ventilation. Patients will be eligible for participation if: 1) adult and 2) receiving intraoperative ventilation during general anesthesia for surgery. Patients receiving ventilation outside of an operating room as well as patients receiving intraoperative ventilation during extracorporeal life support will be excluded
Trial Details
NCT Number NCT06296277
Lead Sponsor Azienda Ospedaliera SS. Antonio e Biagio e Cesare Arrigo di Alessandria
Collaborators: University Of Perugia, University of Chieti, Medical University of Vienna, The Netherlands Cancer Institute, Monash University
Conditions
(from sponsor)		 Surgery, Ventilator Lung, Postoperative Complications
Related terms Postoperative Complications
Enrollment 10,000 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov