Clinical Trials Directory

Trials / Withdrawn

WithdrawnNCT02170558

Enhanced Metal Reduction Techniques for Definitive CT Scanning to Assess Spinal Fusion With TM-Ardis

Evaluating Enhanced Metal Reduction Techniques for Definitive CT Scanning to Assess Spinal Fusion With Trabecular Metal Implants (TM-Ardis)

Status
Withdrawn
Phase
Study type
Observational
Enrollment
0 (actual)
Sponsor
Zimmer Biomet · Industry
Sex
All
Age
18 Years – 85 Years
Healthy volunteers
Not accepted

Summary

To determine if the subject metal reduction software helps to better visualize bone interphase and fusion reliability. Assess whether the appropriate procedural modification facilitates clearer images when implanted with a trabecular metal spinal implant

Detailed description

To determine if the subject metal reduction software helps to better visualize bone interphase and fusion reliability, and assess whether the appropriate procedural modification facilitates clearer images when implanted with a trabecular metal spinal implant.

Conditions

Interventions

TypeNameDescription
DEVICETM- Ardis implant and Metal Reduction CT softwareTM- Ardis implant and Metal Reduction CT software

Timeline

Start date
2014-06-01
Primary completion
2015-12-01
Completion
2015-12-01
First posted
2014-06-23
Last updated
2019-01-24

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT02170558. Inclusion in this directory is not an endorsement.