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OpenTrials
Completed

NCT Number: NCT03030872

Clinical Evaluation of CARESTREAM Vue PACS v12.2 MR Perfusion and Diffusion

The objective of this study is to compare the diagnostic value of MR DSC-Perfusion (Perfusion Module), MR DWI (Diffusion Module) and MR DTI (Diffusion Module) in CARESTREAM Vue PACS ("investigational device") to the Olea Sphere PACS with Perfusion and DWI Modules ("predicate device"). Therefore, there will be several separate objectives depending on the type of acquisition:

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

About this study

Carestream Health, Inc. will investigate the imaging performance of the CARESTREAM Vue PACS v12.2 Magnetic Resonance (MR) Perfusion and Diffusion Weighted Imaging ("investigational device") performance. Evaluation of MR Dynamic Susceptibility Contrast-Enhanced Perfusion Weighted Imaging (DSC-Perfusion), MR Diffusion Weighted Imaging (DWI) and MR Diffusion Tensor Imaging (DTI) was compared to the predicate device, the Olea Sphere PACS with Perfusion and DWI Modules. MR DSC-Perfusion of the brain is a method for evaluating blood flow in the brain and producing optimized parametric maps that help visualize this blood flow. MR DWI is a method to evaluate the motion of water molecules within bodily tissues. MR DTI is an extension of DWI that allows extraction of the diffusion tensor. The purpose of this study is to demonstrate equivalent clinical quality between the investigational and predicate devices using a radiologist evaluation of key metrics which are applicable to MR DSC-Perfusion, MR DWI, and MR DTI images.

Who can participate

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

Inclusion criteria

  • Retrospective patient MR DSC-Perfusion cases with subject/patient 18 years of age or older.
  • Retrospective patient MR DWI with subject/patient 18 years of age or older.
  • Retrospective patient MR DTI cases with subject/patient 18 years of age or older.
  • Informed consent is not required if waiver of consent is approved by the hospital IRB/Ethics Committee

Exclusion criteria

  • Low quality images, or images that are not clinically acceptable for clinical diagnostic reading as determined by the Principal Investigator
  • Subject less than 18 years of age

Treatment and study plan

Investigational software

Device

The study evaluated retrospective de-identified cases that were processed after the imaging procedure had been completed (off-line) using a dedicated workstation.

Primary outcomes

  1. Diagnostic value comparison of Carestream Vue PACS v12.2 MR Perfusion and Diffusion (investigational software) images to the Olea Shere PACS with Perfusion and DWI Modules (predicate software) images.

    Time frame: January 2017

    Diagnostic value of investigational images compared to the diagnostic value of predicate images as assessed by a radiologist evaluation of key metrics.

Sponsors and collaborators

Lead sponsor

Carestream Health, Inc.

Industry

Registry information

Important dates

Study start
2017
Primary completion
2017
Study completion
2017
First posted
Jan 25, 2017
Registry last updated
Nov 14, 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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