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Spontaneous Breathing Mode: A Risk for Hypoxemia During OLV?

Association Between Spontaneous Breathing Mode and Hypoxemia During One-Lung Ventilation Under General Anesthesia

Status
Enrolling by invitation
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07494006
Acronym
OLV
Enrollment
44
Registered
2026-03-27
Start date
2025-07-15
Completion date
2026-12-31
Last updated
2026-03-27

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

Conditions

Hypoxemia During Surgery, Lung Cancer, OLV

Keywords

EIT, OLV, Hypoxemia, lung cancer

Brief summary

Patients undergoing thoracic surgery with one-lung ventilation (OLV) are prone to hypoxemia, which is primarily attributable to pulmonary ventilation-perfusion (V/Q) mismatch. This study will preoperatively assess the distribution of pulmonary ventilation under spontaneous breathing and intraoperatively record the lowest peripheral oxygen saturation (SpO₂) during OLV. The aim is to investigate the correlation between these two parameters. The findings are expected to facilitate the prediction of hypoxemia in thoracic surgical patients undergoing OLV.

Interventions

None listed

Sponsors

Peking University People's Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Age ≥ 18 years * BMI \> 18.5 and \< 30 * Informed consent obtained

Exclusion criteria

* • Inability to use the EIT belt preoperatively * Failure to implement one-lung ventilation during surgery

Design outcomes

Primary

MeasureTime frameDescription
Lowest SpO₂ during OLVPerioperativeWe will record the value of the lowest peripheral oxygen saturation (SpO₂) during intraoperative one-lung ventilation.

Secondary

MeasureTime frameDescription
Postoperative functional statusFollow-up assessments with both questionnaires were conducted at 6 and 12 months postoperatively.After hospital discharge, The Lung Cancer Symptom Scale (LCSS) questionnaires will be administered to patients via telephone by trained follow-up personnel. LCSS typically includes items that evaluate the intensity of symptoms such as cough, dyspnea, pain, fatigue, appetite loss, and insomnia, as well as the impact of these symptoms on daily activities. Each item is rated on a numerical scale, and the total score reflects the overall symptom burden, with higher scores indicating more severe symptoms.
postoperative quality of lifeFollow-up assessments with both questionnaires were conducted at 6 and 12 months postoperatively.After hospital discharge, The Cancer Therapy-Lung (FACT-L) questionnaire will be administered to patients via telephone by trained follow-up personnel. FACT-L is a widely used quality-of-life questionnaire that combines the general FACT-G (General) items with a lung-cancer-specific (LCS) module .Scores are calculated for each domain and a total score, with higher scores indicating better quality of life.

Countries

China

Outcome results

None listed

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