Mechanical Ventilation in Surgical Patients

NCT06296277 · Status: NOT_YET_RECRUITING · Type: OBSERVATIONAL · Enrollment: 10000

Last updated 2025-06-06

No results posted yet for this study

Summary

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

Conditions

  • Surgery
  • Ventilator Lung
  • Postoperative Complications

Interventions

OTHER

Intraoperative mechanical ventilation for surgery

Any IMV during general anesthesia for surgery

Sponsors & Collaborators

  • University Of Perugia

    collaborator OTHER
  • University of Chieti

    collaborator OTHER
  • Medical University of Vienna

    collaborator OTHER
  • The Netherlands Cancer Institute

    collaborator OTHER
  • Monash University

    collaborator OTHER
  • Azienda Ospedaliera SS. Antonio e Biagio e Cesare Arrigo di Alessandria

    lead OTHER

Principal Investigators

  • Gianmaria Cammarota, Prof · Università degli Studi del Piemonte Orientale

  • Rachele Simonte, MD · University Of Perugia

  • Edoardo M De Robertis, Prof · University Of Perugia

  • Sabrine N.T. Hemmes, MD · Department of Anesthesiology The Netherlands Cancer Institute - Antoni van Leeuwenhoek Hospital, Amsterdam, The Netherlands

  • Marcus J Schultz, Prof · Department of Anaesthesia, General Intensive Care & Pain Management, Medical University of Vienna

  • Salvatore M Maggiore, Prof · Department of Anesthesiology and Intensive Care, Ospedale SS Annunziata & Department of Innovative Technologies in Medicine and Odonto-stomatology, Università Gabriele D'Annunzio di Chieti-Pescara, Chieti, Italy

  • Ary Serpa Neto, Prof · Australian and New Zealand Intensive Care Research Centre (ANZIC-RC), School of Public Health and Preventive Medicine, Monash University, Melbourne, Australia

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-09-01
Primary Completion
2026-09-30
Completion
2027-03-01

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06296277 on ClinicalTrials.gov