Powered Echelon Device in VATS Surgery

NCT01843192 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 71

Last updated 2015-06-18

Study results available
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Summary

This study aims to collect real world outcomes of Video-Assisted Thoracoscopic Surgery (VATS) for lung cancer (lobectomy, wedge resection) using ECHELON FLEX™ Powered ENDOPATH® Staplers 45 mm and/or 60 mm (study devices).

Conditions

  • Non-small Cell Lung Cancer (NSCLC)

Interventions

DEVICE

Endocutter

Sponsors & Collaborators

  • Ethicon Endo-Surgery

    lead INDUSTRY

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-05-31
Primary Completion
2014-05-31
Completion
2014-05-31

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01843192 on ClinicalTrials.gov