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NCT Number: NCT07353788

Mechanical Power in One-lung Ventilation

Thoracic surgery usually necessitates one-lung ventilation (OLV) to provide surgical access while maintaining adequate gas exchange. However, OLV is associated with an increased risk of PPCs , a major cause of morbidity and mortality. Mechanical power, a composite parameter incorporating tidal volume, respiratory rate, driving pressure, and flow resistance, has been proposed as a key factor influencing ventilator-induced lung injury (VILI) and postoperative outcome. Understanding the association between mechanical power during OLV and PPCs could provide insights for optimizing intraoperative ventilatory strategies and reducing the burden of PPCs. As OLV inherently alters normal lung mechanics by decreasing functional residual capacity and introducing inequalities in ventilation-perfusion ratio, the complexity of managing mechanical power becomes even more pronounced. Under these altered conditions, the risk of PPC-including atelectasis, pneumonia, and respiratory failure-can be significantly elevated. Factors such as ventilatory settings, lung protection strategies, and the duration of OLV play pivotal roles in influencing mechanical power delivery and thereby impacting lung function recovery post-surgery. Current literature indicates a correlation between inappropriate mechanical ventilation strategies during OLV and increased incidence of PPCs. However, there remains a gap in understanding how precisely mechanical power, as a quantifiable measure, influences patient outcomes following OLV. Therefore, this study aims to investigate the relationship between mechanical power during OLV and the subsequent risk of PPC. By elucidating these dynamics, the findings may inform clinical practices surrounding OLV management, ultimately improving patient safety and outcomes in thoracic surgery.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients aged 18 years or older,
  • ASA physical status I-IV
  • All thoracic surgeries
  • One lung ventilation period >1 hour
  • Patients capable of giving written informed consent

Exclusion criteria

1-Patients undergoing cardiac surgery

Treatment and study plan

Primary outcomes

  1. Number of PPCs during the first five postoperative days, defined according to standard criteria

    Time frame: From enrollment to the end of postoperative 5 th day

    Postoperative pulmonary complications ;(e.g., pneumonia, acute respiratory distress syndrome [ARDS], or prolonged mechanical ventilation).According to StEP-COMPAC group definition [Abbott et al. 2018 Br J Anaesth 2018 May;120(5):1066-1079.]

Secondary outcomes

  1. Threshold mechanical power (J/min)associated with PPCs

    Time frame: From enrollment to postoperative 5 th day

  2. Unscheduled ICU admission rates

    Time frame: From enrollment to postoperative 5 th day

  3. Extra-pulmonary postoperative complications(number of complications)

    Time frame: From enrollment to postoperative 5 th day

  4. Length of ICU stay(day)

    Time frame: up to 5 th day

  5. Length of hospital stay(day)

    Time frame: From enrollment to postoperative 5 th day

Study contacts

Contact information is provided by the study sponsor or research team.

CIGDEM YILDIRIM GUCLU, Prof Dr

CONTACT

[email protected]

+905324576648

Sponsors and collaborators

Lead sponsor

Ankara University

Other

Registry information

Official study title

Postoperative Complications and Outcomes Related to Mechanical Power in One-lung Ventilation- A Multicentre Observational Study

Acronym: POWEROL

Important dates

Study start
2026
Primary completion
2026
Study completion
2026
First posted
Jan 20, 2026
Registry last updated
Jan 20, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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