Clin2
NCT03649490Possibly a fitEnrolling by invitation

Testing new spinal implant materials for XLIF fusion

Degenerative Disc DiseaseSpondylolisthesis

Part of Bones, joints & muscles clinical trials.

This study compares different advanced materials used in a specific spinal fusion surgery (XLIF). It aims to see which implant material helps the bone fuse well and safely over time.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Enrollment
300 people
Ages
18 years to 80 years
Study type
Observational

Who can take part

  • You are age 18 to 80 and getting a planned XLIF-type spinal fusion for wear-and-tear disc disease (degenerative disc disease).
  • Your planned surgery must include the approved NuVasive interbody implant type (Coroent XL PEEK, Modulus 3D-printed titanium, or Cohere XLIF Porous PEEK).
  • Your surgery plan must include screws placed from the back on both sides (and sometimes additional small fusion inside the facet joints).
  • Your spine curve measurement (coronal Cobb angle) must be under 10° before surgery.
  • You must be able to safely have surgery and agree to sign consent to join the study.

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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