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Study on Pulmonary Injury After Esophageal Cancer Surgery

Study on lung injury and its lung microecological mechanism after esophageal cancer surgery

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500112399
Enrollment
Unknown
Registered
2025-11-13
Start date
2025-11-13
Completion date
Unknown
Last updated
2025-11-17

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

Conditions

Acute lung injury

Interventions

No lung injury group:None

Sponsors

Fuzhou University Affiliated Provincial Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1.Age 18-80 years; 2.Diagnosed with esophageal cancer and scheduled for thoracoscopic/laparoscopic esophagectomy; 3.Underwent single-lung ventilation during surgery; 4.Received ICU monitoring for >=12 hours postoperatively; 5.Signed informed consent (patient or legal representative);

Exclusion criteria

Exclusion criteria: 1.Preoperative lung infection or radiation pneumonitis; 2.Interstitial lung disease; 3.ARDS within 6 months or acute respiratory failure with invasive mechanical ventilation within 6 months; 4.A clear history of lung cancer and surgical treatment; 5.Major intraoperative complications that make it impossible to complete the planned surgical plan, such as massive intraoperative bleeding requiring emergency treatment, intraoperative cardiac and respiratory arrest, or severe organ damage caused by surgery; 6.Unplanned intraoperative treatment of the lungs, such as bullectomy or wedge resection of a pulmonary nodule.

Design outcomes

Primary

MeasureTime frame
Pulmonary bacterial flora and metabolites;

Secondary

MeasureTime frame
Left and right lung ventilation ratio;inflammatory factors;Epithelial and endothelial injury markers;Oxidative stress markers;

Countries

China

Contacts

Public ContactBaosong Xie

Fuzhou University Affiliated Provincial Hospital

xbaosong@126.com+86 591 8821 6023

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026