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To compare the recovery of lung function and lung volume after different surgical methods.

To compare the recovery of lung function and lung volume after different surgical methods.

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2300077543
Enrollment
Unknown
Registered
2023-11-13
Start date
2023-07-01
Completion date
Unknown
Last updated
2023-11-21

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

Conditions

Pulmonary nodules

Interventions

Lung segment resection group (Perform segmental lung resection surgery):None
Lung lobe resection group (Perform lung lobe resection surgery):None

Sponsors

Shandong Provincial Hospital Affiliated to Shandong First Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 85 Years

Inclusion criteria

Inclusion criteria: ?Patients with lung tumors who underwent standard lobectomy or standard segmental resection surgery at Shandong Provincial Hospital from December 1, 2021 to January 31, 2023, and were successfully discharged after surgery. ?Pathologically confirmed benign lung tumors and stage IA non-small cell lung cancer. ?Patients who underwent chest CT examination at Shandong Provincial Hospital within 3 months before surgery and 6-12 months after surgery.

Exclusion criteria

Exclusion criteria: ?Patients with postoperative pathology confirmed as small cell lung cancer or non-small cell lung cancer after stage IA. ?Have a history of two or more lung surgeries. ?Those who fail to undergo chest CT examination on time after surgery. ?Patients who experience complications such as pleural effusion, bronchopleural fistula, and atelectasis that affect normal life within six months after surgery.

Design outcomes

Primary

MeasureTime frame
Lung volume;

Countries

the People's Republic of China

Contacts

Public ContactZhongmin Peng

Shandong Provincial Hospital Affiliated to Shandong First Medical University

pzm0803@163.com+86 187 5315 7637

Outcome results

None listed

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