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Optimal Level of PEEP in Protective One-lung Ventilation

Optimal Level of Positive End-expiratory Pressure to Reduce Postoperative Atelectasis After Lung Resection With Protective One-lung Ventilation

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03856918
Enrollment
142
Registered
2019-02-27
Start date
2019-05-28
Completion date
2021-02-28
Last updated
2022-04-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Positive End-expiratory Pressure, Postoperative Atelectasis, Video-assisted Thoracic Surgery

Keywords

Protective ventilation, One-lung ventilation

Brief summary

Protective ventilation strategy has been widely applied in the field of thoracic surgery requiring one-lung ventilation to reduce postoperative pulmonary complications. Low tidal volume, positive end-expiratory pressure (PEEP), and intermittent recruitment maneuver are key components of protective ventilation strategy. Recent evidence suggests that a tidal volume of 4-5 ml/kg should be applied during protective one-lung ventilation. However, optimal level of PEEP is still unclear. This study aims to investigate optimal level of PEEP to minimize postoperative atelectasis by comparing modified lung ultrasound score in patients applied protective one-lung ventilation using PEEP of 3, 6, or 9 cm of water during thoracic surgery.

Interventions

PROCEDUREPEEP 3 cm of water

PEEP of 3 cm of water will be applied during one-lung ventilation.

PROCEDUREPEEP 6 cm of water

PEEP of 6 cm of water will be applied during one-lung ventilation.

PROCEDUREPEEP 9 cm of water

PEEP of 9 cm of water will be applied during one-lung ventilation.

Sponsors

Seoul National University Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Caregiver, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
19 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* Patients undergoing Video-assisted Thoracic Surgery under one-lung ventilation

Exclusion criteria

* Moderate to severe obstructive/restrictive pattern in preoperative pulmonary function test * Chronic kidney disease * Coronary artery disease * Pulmonary hypertension * Bilateral lung surgery * Conversion to thoracotomy * American Society of Anesthesiologists physical status IV or more * Refusal to participate

Design outcomes

Primary

MeasureTime frameDescription
Modified lung ultrasound scorePostoperative 1 hourThe score is calculated by adding up the 12 individual quadrant scores assessed using lung ultrasound.

Secondary

MeasureTime frameDescription
Intraoperative partial pressure of arterial oxygen/fraction of inspired oxygen ratioAverage time of 60-90 minutespartial pressure of arterial oxygen/fraction of inspired oxygen ratio during one-lung ventilation
Postoperative desaturationPostoperative 24 hoursOxygen saturation by pulse oximetry \<95%
plasma Tumor Necrosis Factor-α10 minutes after initiation of one-lung ventilationproinflammatory cytokine
Intraoperative desaturationAverage time of 60-90 minutesOxygen saturation by pulse oximetry \<95% during one-lung ventilation
plasma Interleukin-1010 minutes after initiation of one-lung ventilationanti-inflammatory cytokine
Postoperative pulmonary complicationPostoperative 7 daysComposite outcome of atelectasis, pneumonia, acute respiratory distress syndrome, or pulmonary aspiration
plasma Interleukin-610 minutes after initiation of one-lung ventilationproinflammatory cytokine

Countries

South Korea

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026