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Sublobectomy versus lobectomy for Peripheral non-small cell lung cancer in patients without underlying disease: A multicenter, open-label, nonrandomized, controlled observational study

Sublobectomy versus lobectomy for Peripheral non-small cell lung cancer in patients without underlying disease: A multicenter, open-label, nonrandomized, controlled observational study

Status
Recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2300073309
Enrollment
Unknown
Registered
2023-07-06
Start date
2023-08-01
Completion date
Unknown
Last updated
2023-07-10

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

Conditions

lung cancer

Interventions

Group 1:Sublobectomy
Group 2:lobectomy

Sponsors

Shengjing Hospital Affiliated to China Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 60 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: (1) 1. Enhanced computed tomography (CT) or thin-slice chest CT found isolated lung malignancies less than or equal to 2cm; (2) No suspicious lymph node involvement; (3) between 20 and 60 years old; (4) Preoperative lung function was normal, male FEV1=2500ml, female FEV1=1800ml, FEV1/FVC > 80%; (5) Preoperative blood gas analysis of arterial oxygen partial pressure > 65 torr; (6) Surgical pathology confirmed non-small cell lung cancer, no malignant pleural effusion or pleural spread, no lymph node involvement; (7) Technically feasible lobectomy, segmental resection, wedge resection and lymph node dissection; (8) Obtain the patient's written informed consent.

Exclusion criteria

Exclusion criteria: Exclusion criteria: (1) multiple lung cancers; (2) Tumor history; (3) History of hormone therapy; (4) Have taken aspirin within a week; (5) receiving medication; (6) Cardiovascular and cerebrovascular diseases, endocrine system diseases, immune system diseases; (7) The patient had a history of thoracic surgery; (8) Active bacterial or fungal infection (9) Pregnant or lactating women; (10) interstitial pneumonia, pulmonary fibrosis or severe emphysema; (11) Suffering from mental illness and unable to cooperate.

Design outcomes

Primary

MeasureTime frame
Local recurrence rate;recurrence free survival ;

Secondary

MeasureTime frame
Postoperative respiratory function;Overall survival;adverse event;Completion ratio of pulmonary segment resection and lobectomy;

Countries

China

Contacts

Public ContactZhang Suning

Department of Thoracic Surgery, Shengjing Hospital of China Medical University, Shenyang, Liaoning, China

zhangsn@sj-hospital.org+86 189 4025 1598

Outcome results

None listed

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