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ENROLLING BY INVITATION
NCT05691062
PHASE4

Titanium vs. PEEK Fusion Devices in 1 Level TLIF

Sponsor: Twin Cities Spine Center

View on ClinicalTrials.gov

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.

Official title: A Prospective, Randomized Comparison of Titanium vs. PEEK Fusion Devices in 1 Level TLIF

Key Details

Gender

All

Age Range

18 Years - 70 Years

Study Type

INTERVENTIONAL

Enrollment

80

Start Date

2024-09-01

Completion Date

2028-01-11

Last Updated

2025-06-24

Healthy Volunteers

No

Interventions

DEVICE

Titanium Fusion Device

Titanium fusion device will be utilized for one-level lumbar fusion.

DEVICE

PEEK Fusion Device

PEEK fusion device will be utilized for one-level lumbar fusion.

Locations (1)

Twin Cities Spine Center

Minneapolis, Minnesota, United States