Actively Recruiting

Age: 18Years +
All Genders
ID07099963

Frequency and Severity of Respiratory Acidosis During One-lung Ventilation, a Retrospective Pilot Study Comparing Clinician Settings and the VentilO Application

Led by Laval University · Updated on 2025-08-06

100

Participants Needed

1

Research Sites

26 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are studying patients undergoing thoracic surgery with one-lung ventilation, a type of mechanical ventilation used during these procedures. The study aims to evaluate whether the initial ventilation settings, specifically tidal volume and respiratory rate, are suitable to prevent respiratory acidosis, a condition where carbon dioxide builds up in the blood. The study also compares the ventilation settings chosen by clinicians with those suggested by a smartphone application called VentilO. Participants receive one-lung ventilation with volume-controlled ventilation mode during surgery. The study observes the arterial blood gases during this ventilation and collects data retrospectively. There is no intervention beyond observation, and the study focuses on comparing clinician decisions with app recommendations for ventilation parameters. Participants will have their respiratory status monitored, including acid-base balance and respiratory rate at the start of one-lung ventilation, and respiratory acidosis 20 minutes after ventilation starts. Additional outcomes include the occurrence of hemodynamic shock or hypotension on the day after surgery, hospital length of stay, mechanical ventilation duration, and hospital mortality up to 90 days. The study involves reviewing clinical data without additional procedures, spanning from surgery through up to 90 days of follow-up.

CONDITIONS

Brief Title

Frequency and Severity of Respiratory Acidosis During One-lung Ventilation, a Retrospective Pilot Study to Compare Clinician Settings and Those Proposed by the VentilO Application

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults (≥ 18 years old)
  • Patients intubated and undergoing one-lung ventilation during thoracic surgery
  • Volume-controlled ventilation mode used intraoperatively
Not Eligible

You will not qualify if you...

  • Arterial blood gas data unavailable during one-lung ventilation
  • Missing demographic data (sex, height, actual weight)

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Diagnostic Evaluation

Duration - Surgery day

Participants undergo one-lung ventilation during thoracic surgery where ventilation settings and arterial blood gases are recorded.

1 visit (in-person)

Long-term Monitoring

Duration - Up to 90 days

Participants are observed for clinical outcomes including hemodynamic status, hospital length of stay, mechanical ventilation duration, and mortality.

Follow-up assessments up to 90 days after surgery

Trial Site Locations

Total: 1 location

1

Institut universitaire de cardiologie et de pneumologie de Québec - Université Laval

Québec, Quebec, Canada, G1V4G5

Actively Recruiting

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Research Team

F

Francois Lellouche

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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