Trials / Completed
CompletedNCT04583046
Effects of Iloprost on Pulmonary Oxygenation in Obese Patients During One-lung Ventilation
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 78 (actual)
- Sponsor
- Yonsei University · Academic / Other
- Sex
- All
- Age
- 40 Years – 80 Years
- Healthy volunteers
- Not accepted
Summary
One lung ventilation (OLV) is essential during thoracic surgery. During OLV, intrapulmonary shunt can be increased resulting hypoxemia. Although OLV technique had been advanced so far, hypoxemia during OLV reaches about 10% in spite of inspired oxygen fraction 100%. Iloprost is a prostaglandin analogue used for pulmonary hypertension, which can decrease pulmonary artery resistance by selectively dilating pulmonary artery. In this prospective, randomized, double blind study, the investigator is planning to investigate the effects of iloprost on respiratory physiology (intrapulmonary shunt, deadspace, oxygenation, etc) in obese patients.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | normal saline inhalation | When anesthesia induction finishes, change patients' position from supine to lateral position and measure ABGA, VBGA while two lung is ventilated (T0). After 20 minutes of applying one-lung ventilation, measure ABGA and VBGA (T1). Apply normal saline inhalation for control group and measure ABGA at the time of 20 min after normal saline inhalation has finished (T2). |
| DRUG | iloprost inhalation | When anesthesia induction finishes, change patients' position from supine to lateral position and measure ABGA, VBGA while two lung is ventilated (T0). After 20 minutes of applying one-lung ventilation, measure ABGA and VBGA (T1). Apply iloprost inhalation for iloprost group and measure ABGA at the time of 20 min after iloprost inhalation has finished (T2). |
Timeline
- Start date
- 2020-11-02
- Primary completion
- 2025-09-26
- Completion
- 2025-09-26
- First posted
- 2020-10-12
- Last updated
- 2025-12-01
Locations
1 site across 1 country: South Korea
Source: ClinicalTrials.gov record NCT04583046. Inclusion in this directory is not an endorsement.