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Recruiting NCT07099963

NCT07099963 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

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Clinical Trial Summary
NCT ID NCT07099963
Status Recruiting
Phase
Sponsor Laval University
Condition Thoracic
Study Type OBSERVATIONAL
Enrollment 100 participants
Start Date 2025-08-01
Primary Completion 2025-12

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age N/A
Study Type OBSERVATIONAL
Interventions
one lung ventilation

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.

This trial targets 100 participants in total. It began in 2025-08-01 with a primary completion date of 2025-12.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

One-lung ventilation is a mechanical ventilation method frequently used during several thoracic surgeries. One-lung ventilation requires the use of protective ventilation to limit ventilator-induced injury and reduce postoperative respiratory complications. Protective ventilation during one-lung ventilation is specific since tidal volumes are applied by definition to one lung, and it is recommended to use lower tidal volumes, down to 4 ml/kg of ideal body weight. This approach requires individualized ventilation parameters, which differs from the conventional or two-lung ventilation, and there are no clear recommendations regarding respiratory rate adjustment to ensure adequate gas exchange.

Eligibility Criteria

Inclusion Criteria: * Adults (≥ 18 years old) * Patients intubated and undergoing one-lung ventilation during thoracic surgery * Volume-controlled ventilation mode used intraoperatively Exclusion Criteria: * Arterial blood gas data unavailable during one-lung ventilation * Missing demographic data (sex, height, actual weight)

Contact & Investigator

Central Contact

Francois Lellouche

✉ francois.lellouche@criucpq.ulaval.ca

📞 1-418-656-8711

Frequently Asked Questions

Who can join the NCT07099963 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, studying Thoracic. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07099963 currently recruiting?

Yes, NCT07099963 is actively recruiting participants. Contact the research team at francois.lellouche@criucpq.ulaval.ca for enrollment information.

Where is the NCT07099963 trial being conducted?

This trial is being conducted at Québec, Canada.

Who is sponsoring the NCT07099963 clinical trial?

NCT07099963 is sponsored by Laval University. The trial plans to enroll 100 participants.

ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology