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Safety and Effectiveness Study for a Needle Guidance System in Lung Biopsies

NCT01183182 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 48

Last updated 2012-12-21

No results posted yet for this study

Summary

This study is designed to provide clinical data regarding safety and clinical effectiveness of the ActiSight Needle Guidance System in assisting radiologically guided percutaneous needle biopsy or aspiration of pulmonary lesions, which is a common procedure.

Conditions

  • Lung Diseases

Interventions

DEVICE

ActiSight Needle Guidance System

Three different groups of patients defined per lesion size

Sponsors & Collaborators

  • ActiViews Ltd.

    lead INDUSTRY

Principal Investigators

  • Paul Narinder, MD · University Health Network, Toronto

Study Design

Allocation
NA
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2010-08-31
Primary Completion
2011-02-28
Completion
2011-03-31

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 NCT01183182 on ClinicalTrials.gov