Flow-controlled ventilation - a new and promising method of ventilation presented with a review of the literature.
Szymon Bialka, Piotr Palaczynski, Konstanty Szuldrzynski...
https://pubmed.ncbi.nlm.nih.gov/35142160/Actively Recruiting
Led by Dr Abdurrahman Yurtaslan Ankara Oncology Training and Research Hospital · Updated on 2026-02-06
60
Participants Needed
1
Research Sites
17 weeks
Total Duration
One-lung ventilation OLV is a common technique used during thoracic surgery but can negatively affect lung function and gas exchange. Researchers are studying and comparing two different ventilation methods, flow-controlled ventilation FCV and volume-controlled ventilation VCV, to see how they impact respiratory mechanics and oxygen levels during OLV in adult patients. This multicenter, prospective observational study aims to provide real-world evidence on these ventilation strategies to better understand their benefits and limitations. Patients undergoing thoracic surgery will receive either FCV or VCV as part of their usual care, without any changes made for the study. FCV is a newer method that precisely controls airflow during breathing cycles, while VCV is a commonly used conventional ventilation mode. Data on lung function, airway pressures, oxygenation, and gas exchange will be collected at specific times during both two-lung and one-lung ventilation phases during surgery. Participants will be monitored throughout their surgery with measurements of respiratory mechanics, blood oxygen levels, and other clinical parameters. The study will assess lung compliance, airway pressures, oxygenation capacity, and carbon dioxide elimination during OLV. This information will help improve understanding of lung-protective ventilation during thoracic surgery. The study includes adult patients aged 18 to 80 years and lasts for the duration of the surgical procedure with data collected intraoperatively.
CONDITIONS
Comparison of FCV and VCV in One-Lung Ventilation
Ö
Ökkeş Hakan Miniksar, Assoc.Prof
S
Seher Altınel, Assoc.Prof
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Dr Abdurrahman Yurtaslan Ankara Oncology Training and Research Hospital
Lead Sponsor
Kocaeli City Hospital
Collaborating Sponsor
You may qualify if you...
You will not qualify if you...
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Day of surgery
Participants undergo thoracic surgery requiring one-lung ventilation with ventilation mode determined by routine clinical practice.
1 visit (in-person)
Duration - Intraoperative period during one-lung ventilation
Participants are observed during and after surgery for respiratory mechanics and gas exchange parameters as part of routine clinical care.
Data collected at predefined time points during surgery
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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Szymon Bialka, Piotr Palaczynski, Konstanty Szuldrzynski...
https://pubmed.ncbi.nlm.nih.gov/35142160/Dr Abdurrahman Yurtaslan Ankara Oncology Training and Research Hospital
Lead Sponsor
Kocaeli City Hospital
Collaborating Sponsor