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Assessment of Salbutamol Effect on Arterial Oxygenation in COPD Patients During One-lung Ventilation

Assessment of Salbutamol Effect on Arterial Oxygenation in COPD Patients During One-lung Ventilation

Status
Active, not recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05914285
Enrollment
90
Registered
2023-06-22
Start date
2023-04-25
Completion date
2025-07-21
Last updated
2025-07-01

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

Conditions

Chronic Obstructive Pulmonary Disease, One-lung Ventilation

Brief summary

One-lung ventilation (OLV) is essential part of anesthesia during thoracic procedures. However, OLV induces a drastic increase of intrapulmonary shunt due to maintained pulmonary perfusion through the nonventilated lung, which may result in severe hypoxemia. Although the protective mechanisms of hypoxic pulmonary vasoconstriction favorably modulate pulmonary perfusion to the ventilated lung, the effect is attenuated in patients with history of chronic obstructive pulmonary disease (COPD), which alters compliance of the pulmonary artery. Salbutamol is a selective short-acting beta2-agonist and when inhaled during OLV, it acts selectively on the pulmonary vasculature reducing pulmonary vascular resistance of well-ventilated lung. We hypothesized that inhaled salbutamol would alleviate ventilation-perfusion mismatch during OLV of COPD patients, and aimed to assess the effects of salbutamol on oxygenation in these patients.

Interventions

After the initiation of OLV, 5ml of normal saline is inhaled for 20 minutes using ultrasonic nebulizer, which is connected to the inspiratory limb of the ventilator system. Arterial blood gas analysis is performed 30 minutes after the completion of drug inhalation.

DRUG2.5mg (2.5ml) of inhaled salbutamol and 2.5ml of inhaled normal saline

After the initiation of OLV, mixture of salbutamol 2.5mg and normal saline 2.5ml is inhaled for 20 minutes using ultrasonic nebulizer, which is connected to the inspiratory limb of the ventilator system. Arterial blood gas analysis is performed 30 minutes after the completion of drug inhalation.

Sponsors

Yonsei University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

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

Inclusion criteria

* Patient age 40\ 80yrs, scheduled for videoscope-assisted pulmonary lobectomy * American Society of Anesthesiologists Class III 또는 IV * Moderate or more severe COPD according to GOLD criteria (FEV1/FVC\<70%, FEV1\<80%)

Exclusion criteria

* New York Heart Association class \>II * AST level ≥100 IU/mL or ALT ≥ level 50 IU/L * Creatinine clearance \< 30mL/min * History of severe coronary artery occlusive disease, unstable angina, or recent myocardial infarction within 6 months * History of pulmonary hypertension or pulmonary edema * History of cerebrovascular accident within 3 months

Design outcomes

Primary

MeasureTime frameDescription
PaO2 (partial pressure of arterial oxygen) to FiO2 (fraction of inspired oxygen) ratio (P/F ratio)Thirty minutes after the completion of drug inhalationThe P/F ratio is a widely-used objective tool to identify hypoxemic respiratory failure when supplemental oxygen has been administered. It can be used to evaluate the effect of salbutamol on oxygenation during OLV.

Countries

South Korea

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 28, 2026