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Is Video-assisted Thoracoscopic Lobectomy a Clinical Alternative for Surgically Resectable Pathologic N2 NSCLC Patients

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

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03613467
Enrollment
2145
Registered
2018-08-03
Start date
2018-07-04
Completion date
2018-07-06
Last updated
2018-08-09

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

Conditions

Non-small Cell Lung Cancer

Keywords

Vedio-assisted thoracoscopic lobectomy, Thoracotomy lobectomy, Real-world evidences;, pN2 NSCLC

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.

Interventions

Patients who received lobectomy by video-assisted thoracoscopic surgery

PROCEDUREThoracotomy lobectomy

Patients who received lobectomy by thoracotomy

Sponsors

LinkDoc Technology (Beijing) Co. Ltd.
CollaboratorINDUSTRY
Tang-Du Hospital
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
RETROSPECTIVE

Eligibility

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

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

Design outcomes

Primary

MeasureTime frameDescription
Overall survival2014-2018Overall survival

Secondary

MeasureTime frameDescription
Duration of hospital stay [Perioperative outcomes]2014-2017Duration of hospital stay \[Perioperative outcomes\]
Postoperative 30 and 90 days [Perioperative outcomes]2014-2017Postoperative 30 and 90 days \[Perioperative outcomes\]
Drainage time [Perioperative outcomes]2014-2017Drainage time \[Perioperative outcomes\]
Intraoperative blood loss [Perioperative outcomes]2014-2017Intraoperative blood loss \[Perioperative outcomes\]
Postoperative complications [Perioperative outcomes]2014-2017Postoperative complications \[Perioperative outcomes\]

Other

MeasureTime frameDescription
Propensity score matching analysis of perioperative outcomes2014-2018Propensity score matching analysis of perioperative outcomes
Overall survivals in the subgroups stratified by T staging2014-2018Overall survivals in the subgroups stratified by T staging
Propensity score matching analysis of impact factors for postoperative mortality within 30/90 days2014-2018Propensity score matching analysis of impact factors for postoperative mortality within 30/90 days
Propensity score matching analysis of impact factors for overall survival2014-2018Propensity score matching analysis of impact factors for overall survival
Overall survivals in the subgroups stratified by neoadjuvant therapy2014-2018Overall survivals in the subgroups stratified by neoadjuvant therapy
Overall survivals in the subgroups stratified by number of lymph node station involved2014-2018Overall survivals in the subgroups stratified by number of lymph node station involved
Impact factors for overall survival2014-2018Impact factors for overall survival
Impact factors for postoperative mortality within 30/90 days2014-2017Impact factors for postoperative mortality within 30/90 days
Propensity score matching analysis of overall survival2014-2018Propensity score matching analysis of overall survival

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026