Mechanical Power and Pulmonary Complications in CABG Surgery

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorFusun Gozen

About this trial

This prospective observational study evaluates the association between intraoperative mechanical power (MP) - a composite measure of the total energy delivered to the lungs during mechanical ventilation - and postoperative pulmonary complications (PPCs) and prolonged mechanical ventilation in adult patients undergoing elective coronary artery bypass graft (CABG) surgery with cardiopulmonary bypass (CPB). Intraoperative ventilatory parameters including tidal volume, respiratory rate, airway pressures, and PEEP will be recorded and used to calculate MP and driving pressure (DP). No additional interventions will be applied beyond standard clinical care.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Age 18 years or older

Scheduled for elective, first-time isolated CABG surgery

Use of cardiopulmonary bypass (CPB)

Intraoperative mechanical ventilation applied under general anesthesia with recordable ventilator data

Disqualifiers

Emergency cardiac surgery

Off-pump CABG (without CPB)

Preoperative requirement for invasive mechanical ventilation

Advanced chronic lung disease

Trial population

Adult patients undergoing elective isolated CABG surgery with cardiopulmonary bypass at a single tertiary cardiac surgery center

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • Intraoperative Mechanical Ventilation Monitoring

    Other intervention

    Intraoperative ventilatory parameters (tidal volume, respiratory rate, plateau pressure, PEEP) are routinely recorded during CABG surgery. Mechanical power and driving pressure are calculated from these parameters. No additional intervention is applied beyond standard clinical care.

Treatment groups

110 Participants
are divided into 1 treatment group
Group A: CABG Patients1 intervention

Trial outcomes

Primary outcomes

1

Postoperative Pulmonary Complication

Occurrence of at least one of the following within the first 48 hours postoperatively: atelectasis, pleural effusion, pneumonia, prolonged oxygen requirement, need for non-invasive ventilation (NIV), or re-intubation

Time frame
Within the first 48 hours postoperatively

Secondary outcomes

1

Prolonged Mechanical Ventilation

Duration of mechanical ventilation greater than 24 hours

Time frame
Up to 7 days postoperatively

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Fusun Gozen

Lead sponsor

Bursa Yuksek Ihtisas Training and Research Hospital

Sponsor institution

This trial is not recruiting at the moment. You can still explore other options: