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Clinical Trial

Lumbar Fusion With Porous Versus Non-Porous Cages

NCT: NCT05583864 · ACTIVE_NOT_RECRUITING

NCT IDNCT05583864
StatusACTIVE_NOT_RECRUITING
Start Date2022-11-01
SponsorFrancis Farhadi (OTHER)
First posted
Last updated

Brief Summary

The objective of this single site, randomized controlled trial is to assess and compare radiographic and clinical outcomes in patients who are to undergo lumbar interbody fusion procedures (TLIF), supplemented with pedicle screw instrumentation, using one of the following interventions: 1. Porous titanium cages 2. Non-porous titanium-coated poly-ether-ether-ketone (PEEK) cages.

Official Source

View on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.

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