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OpenTrials
Completed

NCT Number: NCT01972386

EBUS/Spectrum Analysis

To evaluate the clinical benefit of spectrum analysis of endobronchial ultrasound images of lymph nodes during EBUS TBNA for lymph node staging in patients with lung cancer.

Completed

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

University Health Network

Toronto, Ontario, M5G 2C4, Canada

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Ages 18 years or older
  • Patients with known or suspected lung cancer who require EBUS-TBNA for lymph node staging

Exclusion criteria

  • Patients who are deemed on clinical grounds not to be medically fit for a bronchoscopy
  • Inability to give informed consent
  • Patients who are pregnant

Treatment and study plan

Spectrum Image Analysis using a Linear Array Ultrasound Bronchoscope

Device

Primary outcomes

  1. Lymph Node Staging

    Time frame: Pathology report will be completed as soon as possible after the procedure. (Within one year)

    The lymph node staging will be determined by the pathology report of the biopsy taken from the patients lymph node(s).

Sponsors and collaborators

Lead sponsor

University Health Network, Toronto

Other

Registry information

Official study title

Spectrum Image Analysis of Lymph Nodes During Endobronchial Ultrasound-Guided (EBUS) Transbronchial Needle Aspiration (TBNA) in Patients With Lung Cancer

Important dates

Study start
2013
Primary completion
2015
Study completion
2016
First posted
Oct 30, 2013
Registry last updated
Feb 23, 2018

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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