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Safety & Accuracy Study of the ActiSight Needle Guidance System in Patients Undergoing CT-Guided Percutaneous Chest Aspiration and Biopsy

NCT00819533 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 40

Last updated 2009-12-29

No results posted yet for this study

Summary

This study is designed to evaluate preliminary safety and accuracy of the ActiSight™ Needle Guidance System in patients undergoing CT-guided lung aspiration or biopsy. This image guidance system uses a combination of CT scans and camera images to help guide a biopsy needle to a lung lesion. The system displays a simulated image of a biopsy needle and its estimated path for the biopsy.

Conditions

  • Biopsy

Interventions

DEVICE

sensor (ActiSight™ Needle Guidance System)

Patients will have their lung sample obtained under CT and ActiSight needle guidance system

Sponsors & Collaborators

  • ActiViews Ltd.

    lead INDUSTRY

Principal Investigators

  • Narinder Paul, MD · University Health Network, Toronto General Hospital

  • Uri Shreter, Ph.D. · ActiViews Ltd.

Study Design

Allocation
NON_RANDOMIZED
Purpose
DIAGNOSTIC
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2008-01-31
Primary Completion
2009-10-31
Completion
2009-10-31

Countries

  • Canada

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 NCT00819533 on ClinicalTrials.gov