Trial reportScientific reports2026
Mechanical power guided lung protective ventilation in acute respiratory failure using the VentCoach approach.
Trial report in Scientific reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT07294768 (Mechanical Power-Guided Lung Protective Ventilation), which is not on this map. Not yet cited in PubMed.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Mechanical Power-Guided Lung Protective Ventilation (VentCoach) in Acute Hypoxemic and/or Hypercapnic Respiratory Failure: A Feasibility, Double Arm, Single-blinded Study
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
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Authors and funding
7 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Mechanical power (MP) is increasingly recognized as a unifying variable that encapsulates ventilator-derived factors contributing to ventilator-induced lung injury. However, its clinical application remains limited by several challenges, including the lack of accessible real-time MP monitoring. This study aims to demonstrate the feasibility and safety of an electronic health record-integrated, MP-guided, and respiratory therapist (RT)-driven lung-protective ventilation (LPV) protocol (VentCoach). Single-center, single-blinded, randomized controlled feasibility trial utilizing block randomization to assign participants to either the standard care or VentCoach arm. Adult patients with acute hypoxemic and/or hypercapnic respiratory failure requiring intubation, admitted to medical or mixed medical-surgical ICUs at a tertiary care center in Rochester, Minnesota, were included in the study. The standard care arm received RT-driven lung-protective ventilation (LPV). The VentCoach arm received MP-guided adjustments to maintain mechanical power < 12 J/min while ensuring adequate gas exchange. Seventeen patients (n = 9 standard care, n = 8 VentCoach) were enrolled, demonstrating the feasibility of VentCoach without adverse events or workflow disruptions. No significant differences were observed in mortality, extubation time, dyssynchrony, or the use of sedation, analgesia, neuromuscular blockade, or vasoactive agents. The VentCoach group showed trends toward lower sedation requirements (− 25.9 mg/hour vs. +18.1 mg/hour, p = 0.09) and greater reduction in mechanical power over 24 h (− 2.0 J/min vs. + 0.6 J/min, p = 0.40), although these differences were not statistically significant. This feasibility study demonstrated practical implementation of the VentCoach protocol in a critical care setting, with no protocol-related adverse events or workflow disruptions in this limited cohort. While non-inferiority to standard lung-protective ventilation was observed, relationships between MP thresholds and clinical outcomes remain uncertain; directional signals support further study. Larger trials are needed to evaluate safety, MP reduction, and patient-centered outcomes (ClinicalTrials.gov Identifier: NCT07294768, Registration Date and Last Public Release: 12/08/2025).
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