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Clinical Trials/NCT03613467
NCT03613467
Completed
Not Applicable

Vedio-assisted Thoracoscopic Lobectomy vs Open Lobectomy for Patients With Surgically Resectable Pathologic N2 NSCLC

Tang-Du Hospital10 sites in 1 country2,145 target enrollmentJuly 4, 2018

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Non-small Cell Lung Cancer
Sponsor
Tang-Du Hospital
Enrollment
2145
Locations
10
Primary Endpoint
Overall survival
Status
Completed
Last Updated
7 years ago

Overview

Brief Summary

The study was designed to compare the safety and effectiveness of vedio-assisted thoracoscopic lobectomy with open lobectomy for patients with surgically resectable pathologic N2 non-small cell lung cancer

Detailed Description

The is a multi-center retrospective study. Patients with pathologic N2 NSCLC who underwent VATS or open lobectomy between 2014 and 2017 were included into this study. Clinical data on patient demographic, clinical characteristics, treatment and clinical outcomes will be collected to evaluate the safety and effectiveness of video-assisted thoracoscopic lobectomy for pathologic N2 NSCLC.

Registry
clinicaltrials.gov
Start Date
July 4, 2018
End Date
July 6, 2018
Last Updated
7 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Tang-Du Hospital
Responsible Party
Principal Investigator
Principal Investigator

lixiaofei

Professor

Tang-Du Hospital

Eligibility Criteria

Inclusion Criteria

  • Patients with age \> 18 years old;
  • Patients with pathologically diagnosed non-small cell lung cancer;
  • Patients underwent lobectomy by either VATS or thoracotomy between 2014 and 2017;
  • Patients who received lymphadenectomy for all accessible lymph nodes;
  • Patients with N2 lymph nodes (+) after surgeries;

Exclusion Criteria

  • Patients with second primary tumors or multiple primary tumors;
  • Patients who received chest surgeries before hospitalization;
  • Patients with superior pulmonary sulcus tumor

Outcomes

Primary Outcomes

Overall survival

Time Frame: 2014-2018

Overall survival

Secondary Outcomes

  • Postoperative 30 and 90 days [Perioperative outcomes](2014-2017)
  • Drainage time [Perioperative outcomes](2014-2017)
  • Duration of hospital stay [Perioperative outcomes](2014-2017)
  • Postoperative complications [Perioperative outcomes](2014-2017)
  • Intraoperative blood loss [Perioperative outcomes](2014-2017)

Study Sites (10)

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