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NCT05691062
Titanium vs. PEEK Fusion Devices in 1 Level TLIF
Conditions: Spine Fusion, Lumbar Spondylolisthesis, Lumbar Stenosis
Sex: All
Ages: 18 Years – 70 Years
Phase: PHASE4
Enrollment: 80
Sponsor: Twin Cities Spine Center
Location: United States
Summary
The objective of this study is to evaluate and follow the clinical and radiographic outcomes of patients undergoing 1 level TLIF randomized to either a titanium or a PEEK spacer to 24 months after surgery.
Eligibility Criteria
Inclusion CriteriaPatients undergoing 1 level TLIF for the treatment of lumbar stenosis and spondylolisthesis who have failed at least 6 weeks of non-operative treatment.Patients between 18-70 years of age at the time of surgery.Exclusion CriteriaPatients under 18 or over 70 years of age at the time of surgery.Patients undergoing more than 1 level of surgery.Patients who have had prior lumbar fusion.Patients requiring surgery for the management of infection, tumor, or trauma.Patients who are pregnant.
Source: ClinicalTrials.gov (NCT05691062). StuddyBuddy aggregates publicly available trial information.
