CompletedNot applicableNCT01843192

Powered Echelon Device in VATS Surgery

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).

Checked against the public recordLast updated Jun 18, 2015 · Source: ClinicalTrials.gov

StatusCompleted
PhaseNot applicable
U.S. locations4
SponsorEthicon Endo-Surgery
01
Study overview

What this study is about

Purpose
Not specified
Study type
Observational
Phase
Not applicable
Sponsor
Ethicon Endo-Surgery
Interventions being studied
Device: Endocutter
02
Explore related studies

How this study is categorized

These labels come from structured fields and exact terms in the public record.

03
Public criteria

Who may be able to participate

Inclusion Criteria: * Suspected or confirmed NSCLC (up to and including Stage II) * Scheduled for lung resection surgery (lobectomy or wedge resection) involving only one lobe of the lung * Performance status 0-1 (Eastern Cooperative Oncology Group classification) * ASA score \< 3 * No prior history of VATS or open lung surgery * Willing to give consent and comply with study-related evaluation and treatment schedule Exclusion Criteria: * Active bacterial infection or fungal infection; * Systemic administration (intravenous or oral) of steroids (within 30 days prior to study procedure) * Chemotherapy or radiation therapy for lung cancer may not be performed for 30 days prior to the procedure * Scheduled concurrent surgical procedure other than wedge resection or lobectomy (central venous access - e.g. port placement, mediastinoscopy with lymph node sampling, and VATS lymphadenectomy are allowed) * Pregnancy * Physical or psychological condition which would impair study participation; * The patient is judged unsuitable for study participation by the Investigator for any other reason; or * Unable or unwilling to attend follow-up visits and examinations

Important: This is the sponsor’s public criteria, not a determination of eligibility. The study team must review your individual situation.

04
Study sites

U.S. locations

  • Dignity Health, St. Joseph's Hospital & Medical CenterPhoenix, Arizona
  • Massachusetts General HospitalBoston, Massachusetts
  • Washington University School of MedicineSt Louis, Missouri
  • Vanderbilt UniversityNashville, Tennessee

Source and freshness
Processed from ClinicalTrials.gov. Last public update: Jun 18, 2015. Always confirm current availability with the study team.

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