Is a
Clinical Study attributes
NCT Number
Health Conditions in Trial
Trial Recruitment Size
1080
Trial Sponsor
Clinical Trial Start Date
November 1, 2022
0Primary Completion Date
2025
0Study Completion Date
2026
0Clinical Trial Study Type
Interventional0
Interventional Trial Purpose
Treatment0
Intervention Type
Device0
Intervention Name
CONDUIT Porous Titanium Spinal Cage0
PROTI 360 Titanium-Coated PEEK Spinal Cage0
Interventional Trial Phase
Not Applicable0
Participating Facility
Official Name
Lumbar Fusion With Porous Titanium Versus Non-Porous Titanium-Coated PEEK Interbody Cages - A Randomized Controlled Trial0
Last Updated
October 5, 2023
0Allocation Type
Randomized0
Intervention Model
Parallel Assignment0
Masking Type
Triple0
Masked Party
Participant0
Investigator0
Care Provider0
Study 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.
Timeline
No Timeline data yet.
Further Resources
No Further Resources data yet.
