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NCT Number: NCT07044089

Lung Protective Ventilation and Driving Pressure Guided PEEP Titration in CABG Surgery

Our aim in this study is to compare fixed and individualized PEEP (driving pressure guided ) application for intraoperative lung protective ventilation in patients undergoing on-pump CABG surgery.

Researcher aimed to compare the effects of two different PEEP application methods on intraoperative hemodynamics, respiratory mechanics, and gas exchange, as well as postoperative extubation times, respiratory complications (atelectasis, need for non invasive mechanical ventilatıon, need for re-entubatıon) length of stay in the intensive care unit, and discharge times.

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Key information

Age range

18 year–70 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Kocaeli University Faculty of Medicine

Kocaeli, izmit, 41100, Turkey (Türkiye)

Location status: Recruiting

Location contact

Zeynep Açık

CONTACT

[email protected]

05077367990

About this study

The primary goal of the researchers: To compare the effects of fixed PEEP versus driving pressure guided individualized PEEP in lung protective mechanical ventilation during on-pump open heart surgery effect of PaO2/ FiO2 ratio end of surgery.

The secondary goals of the researchers: To compare intraoperative hemodynamics, lung compliance and airway pressures, extubation time and respiratory complications [development of atelectasis, need for noninvasive mechanical ventilation (high-flow nasal cannula or CPAP application), need for re-intubation], length of stay in the ICU and discharge times.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Patients scheduled for elective on-pump coronary artery bypass graft surgery via median sternotomy
  • Patients between the ages of 18 and 70
  • ASA (American Society of Anesthesiologists) physical status classification II-III

Exclusion criteria

  • Patients with an ejection fraction below 35%
  • Patients who did not consent to participate in the study
  • Patients undergoing emergency surgery
  • Patients who are allergic to the anesthetic drugs used
  • Patients who have undergone lung resection
  • Those with a history of mechanical ventilation in the 2 months before surgery
  • Patients who have undergone total circulatory arrest and deep hypothermia
  • Patients with obstructive sleep apnea syndrome requiring long-term ventilation assistance
  • Morbid obesity (Body Mass Index>35kg/m2)
  • Patients with refractory hypoxemia (arterial oxygen saturation below 88% despite 100% oxygen inhalation)
  • COPD (FEV1<70%)
  • Patients with chronic renal failure (serum creatine>1.8 mg/dl)
  • Anemia (Hg<10 gr/dl)
  • Patients who have had an intraaortic balloon pump placed.

Treatment and study plan

Primary outcomes

  1. Effects on intraoperative oxygenation, hemodynamics, lung compliance and airway pressures

    Time frame: First one day

    Data will be recorded during surgery and the first 24 hours after extubation.

Study contacts

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

Tülay Çardaközü, PROFESSOR

CONTACT

[email protected]

+905323262342

Zeynep Açık, MD

CONTACT

[email protected]

+905077367990

Sponsors and collaborators

Lead sponsor

Kocaeli University

Other

Registry information

Official study title

Comparison of Individualized PEEP Application Versus Fixed PEEP Application for Lung-Protective Ventilation in Patients Undergoing On-Pump Coronary Artery Bypass Grafting Surgery

Important dates

Study start
2025
Primary completion
2027
Study completion
2027
First posted
Jun 29, 2025
Registry last updated
Aug 8, 2025

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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