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Clinical Trial Summary

The purpose of this study is to collect feedback on imaging guidance adequacy from physicians who use the OEC™ Elite CFD Mobile Fluoroscopy System—Motorized Configuration to perform surgical procedures for which the use of mobile fluoroscopy is prescribed per standard of care.

Up to 40 eligible subjects will be enrolled and have their clinically indicated procedure completed using the investigational device.

Following completion of each subject's procedure, the investigators will complete a User Survey specific to the workflow and guidance adequacy of the OEC Elite device. The survey will consist of a series of questions on the use of the system as well as anonymized image data.

After all subjects' procedures are completed at a given site, the site investigator will review survey data from the study subjects enrolled at the site and document his/her assessment of the overall acceptability of the system for use in a clinical environment.

There is no statistical hypothesis being tested in this study. Results will be summarized using descriptive statistics.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms

  • Interventional Vascular Conditions

NCT number NCT03417713
Study type Observational
Source GE Healthcare
Contact
Status Completed
Phase
Start date April 4, 2018
Completion date May 29, 2018

See also
  Status Clinical Trial Phase
Terminated NCT03096483 - Clinical Evaluation of the OEC Elite Vascular Mobile Fluoroscopy System N/A