Actively Recruiting

Age: 18Years - 70Years
All Genders
Healthy Volunteers
NCT07044089

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

Led by Kocaeli University · Updated on 2025-08-08

86

Participants Needed

1

Research Sites

110 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

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

Who Can Participate

Age: 18Years - 70Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • 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
Not Eligible

You will not qualify if you...

  • 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

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Kocaeli University Faculty of Medicine

Kocaeli, izmit, Turkey (Türkiye), 41100

Actively Recruiting

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Research Team

Z

Zeynep Açık, MD

CONTACT

T

Tülay Çardaközü, PROFESSOR

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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