Skip to content

Lung Atelectasis Improvement Through Positive End Expiratory Pressure During Anesthetic Induction

Lung Atelectasis Improvement Through Positive End Expiratory Pressure During Anesthetic Induction: a Randomized Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06900426
Enrollment
120
Registered
2025-03-28
Start date
2025-03-28
Completion date
2025-04-28
Last updated
2025-05-29

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

Conditions

Lung Injury, Acute

Brief summary

Anesthetic induction could lead to lung atelectasis, increase intrapulmonary shunt, and potentially impair oxygenation. The study aimed to validate that a positive end-expiratory pressure (PEEP) of 10 cmH2O could reduce lung atelectasis, comparing to 0 or 5 cmH2O with limited overdistension.

Detailed description

General anesthesia may introduce lung atelectasis, which causes an increase in intrapulmonary shunt, and impairs oxygenation, even in the lung-healthy subjects. The magnitude of shunt is correlated with the formation of pulmonary atelectasis. The study aimed to validate that a positive end-expiratory pressure (PEEP) of 10 cmH2O could reduce lung atelectasis, comparing to 0 or 5 cmH2O with limited overdistension. Surgical patients with healthy lungs were randomly assigned to receive 0, 5 or 10 cmH2O PEEP (PEEP0, PEEP5 and PEEP10 groups). Anesthetic induction was performed by certified registered anesthesiologists, during which the patients were mechanically ventilated using the volume-controlled mode. Electrical impedance tomography (EIT) was used to dynamically assess the lung atelectasis during anesthetic induction (spontaneous, mask, and endotracheal intubation ventilation). The primary outcome was the dorsal change of end expiratory lung impedance (△EELI) after 2 mins anesthetic induction. The secondary outcome was driving pressure, EIT-derived ventilation homogeneity, hemodynamics and PaO2/FiO2.

Interventions

OTHER10 PEEP

Using 10cmH2O PEEP during anesthetic induction monitored by EIT.

OTHERZEEP

No PEEP

OTHER5PEEP

Using 5cmH2O PEEP

Sponsors

Fudan University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
Yes

Inclusion criteria

* between 18 and 80 years * scheduled for elective non-cardiothoracic cancer surgery * general anesthesia.

Exclusion criteria

* acute or chronic respiratory disorders, such as chronic obstructive pulmonary disease (COPD) or asthma; * a history of lung surgery * a high risk of reflux and aspiration * a requirement for awake intubation * facial or thoracic deformities * the presence of implants, such as cardiac pacemakers * pregnant

Design outcomes

Primary

MeasureTime frameDescription
the dorsal △EELV after 2 minutes anesthetic induction2 minutes after anesthetic inductionThe primary outcome was the dorsal △EELV after 2 minutes anesthetic induction (endotracheal intubation ventilation) monitored by EIT.

Secondary

MeasureTime frameDescription
driving pressure2 minutes after anesthetic inductionPplat - PEEP
GI2 minutes after anesthetic inductionGlobal imhomogeneity monitored by EIT
CoV2 minutes after anesthetic inductionThe central of ventilation monitored by EIT
hemodynamicsDuring anesthetic inductionBlood pressure
PaO2/FiO2During anesthetic inductionPaO2/FiO2 during anesthetic induction

Countries

China

Outcome results

None listed

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