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

Withdrawn before enrolling

Conditions studied: Degenerative Disc Disease

In brief

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

Key facts

Study ID

NCT02170558

Run by

Zimmer Biomet

People needed

0

Starts

2014-06-01

Expected to finish

2015-12-01

Last updated by the study team

2019-01-24

Who can join

Age: 18 and older, up to 85. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• A signed informed consent.
• Male or non-pregnant female scheduled for Trabecular Metal (TM - Ardis) implant, single level lumbar.
• Participant must be at least 18 years of age.

You may not qualify if…

• Patient is pregnant Patient is unable to comprehend the requirements of the study.
• Patient is unable to undergo scanning (due to body habitus, inability to comply with positioning requirements, etc.).

Where it is running

• St Alphonsus Regional Medical Center — Boise, Idaho, United States

Full record on ClinicalTrials.gov

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