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Pilot Study Comparing Diagnostic Imaging Versus Tomosynthesis in Detection of Hip, Wrist or Tibia Injury

NCT01927575 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 1

Last updated 2020-06-04

Study results available
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Summary

To acquire and build a library of image sets to determine if Fuji's TOMO imaging device can replace or compliment current imaging standards to assess patients with hip, wrist or tibia injuries.

Conditions

  • Wrist Injury
  • Tibial Fracture
  • Hip Injury

Interventions

DEVICE

Standard X-Ray + CT

Standard of Care X-Ray Imaging + CT

DEVICE

Standard X-Ray + MRI

Standard of Care X-Ray Imaging + MRI

DEVICE

TOMO

Fujifilm Digital Radiographic AcSelerate CsI System with Tomosynthesis

Sponsors & Collaborators

  • Fujifilm Medical Systems USA, Inc.

    lead INDUSTRY

Principal Investigators

  • Davide Bova, MD · Loyola University Chicago

Study Design

Allocation
NON_RANDOMIZED
Purpose
DIAGNOSTIC
Masking
NONE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-09-30
Primary Completion
2014-04-30
Completion
2014-04-30

Countries

  • United States

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 NCT01927575 on ClinicalTrials.gov