GE Healthcare VolumeRAD Lung Nodule Detection Study

Sponsor
American College of Radiology - Image Metrix (Industry)
Overall Status
Completed
CT.gov ID
NCT00963651
Collaborator
GE Healthcare (Industry)
187
4
47
46.8
1

Study Details

Study Description

Brief Summary

To perform a multiple reader, multiple case (MRMC) observer study assessing the detection performance of VolumeRAD tomosynthesis of the chest in detecting lung nodules.

Condition or Disease Intervention/Treatment Phase
  • Device: Chest tomosynthesis and X-ray

Detailed Description

Digital tomosynthesis is a form of limited angle tomography that creates a series of section images using a conventional x-ray tube and generator, a digital detector, and appropriate reconstruction software. It creates section images from a series of projection images acquired as the x-ray tube moves along a prescribed path. Because tomosynthesis can minimize the visual presence of overlying anatomy - the ribs, for example - it has the potential to improve the detection of lesions such as pulmonary nodules when compared with conventional chest radiography.

The primary aim of this study is to determine whether the use of VolumeRAD tomosynthesis, in addition to CxR, increases physician accuracy in the detection of lung nodules between 3mm and 20mm in diameter when compared to conventional posterior-anterior (PA) and lateral (LAT) chest radiography (CxR). This aim will be addressed by measuring free-response performance of experienced (with VolumeRAD), blinded expert readers' detection performance. Specifically, we will compare detection performance, as measured by the area under the alternative free response receiver operating characteristic (AFROC) curve, among readers viewing PA and LAT chest X-rays versus VolumeRAD tomosynthesis. The nodule will be the unit of analysis.

Study Design

Study Type:
Observational
Actual Enrollment :
187 participants
Observational Model:
Case-Only
Time Perspective:
Cross-Sectional
Official Title:
GE Healthcare VolumeRAD Lung Nodule Detection Study
Study Start Date :
Aug 1, 2009
Actual Primary Completion Date :
Jul 1, 2013
Actual Study Completion Date :
Jul 1, 2013

Arms and Interventions

Arm Intervention/Treatment
Suspicion of pulmonary nodules

Eligible participants will include those referred for x-ray computed tomography (CT) of the chest for suspicion of a pulmonary nodule or other unrelated reasons.

Device: Chest tomosynthesis and X-ray
VolumeRAD tomosynthesis; Conventional Chest X-ray; Dual energy (bone and soft tissue PA chest images)

Outcome Measures

Primary Outcome Measures

  1. Multi-reader, multi-case Receiver Operating Characteristics (ROC) methodology. [Post accrual of 210 participants]

    The primary objective of this study is to determine if the use of VolumeRAD tomosynthesis increases the accuracy of the detection of lung nodules between 3mm and 20mm in diameter when compared to conventional PA and lateral chest radiography alone.

Secondary Outcome Measures

  1. Actionability classification accuracy of all modalities [Multipe reader, multiple case reader study]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Scheduled for chest CT as part of their needed medical care;

  • If available, individuals who have had previous imaging to suggest they fulfill the needs of the study;

  • 18 years of age, or older;

  • In good enough physical condition to stand motionless and hold their breath during the image acquisition procedures.

Exclusion Criteria:
  • Children under 18 years of age;

  • Women who are pregnant or who suspect they may be pregnant;

  • Individuals who on previous imaging are shown to have objects in or around the lungs that might produce substantial artifacts that would obscure pulmonary nodules;

  • Individuals who on recent imaging had active lung or pleural disease that would obscure pulmonary nodules;

  • Individuals with more than 5 pulmonary nodules between 5mm and 20mm in diameter in either right or left lung.

  • Individuals suspected to have more than 15 total nodules between 3mm and 20mm. NOTE that up to 20 nodules between 3mm and 20mm will be allowed in the final study sample.

Contacts and Locations

Locations

Site City State Country Postal Code
1 University of Michigan Ann Arbor Michigan United States 48103
2 Duke University Medical Center Durham North Carolina United States 27705
3 University of Washington Medical Center Seattle Washington United States 98195
4 Sahlgrenska University Hospital Gothenburg Sweden SE-413 45

Sponsors and Collaborators

  • American College of Radiology - Image Metrix
  • GE Healthcare

Investigators

  • Principal Investigator: James Dobbins, MD, Duke University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
American College of Radiology - Image Metrix
ClinicalTrials.gov Identifier:
NCT00963651
Other Study ID Numbers:
  • GE-VORTEX
  • GE 2901
First Posted:
Aug 21, 2009
Last Update Posted:
Jul 24, 2013
Last Verified:
Jul 1, 2013
Keywords provided by American College of Radiology - Image Metrix
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jul 24, 2013