Stopped: The patient population is too low to conduct the study in a feasible and meaningful amount of time.
This is a prospective, randomized clinical trial of patients undergoing 1-level lateral lumbar spinal fusion. This study seeks to randomize patients indicated for Lateral Lumbar Interbody Fusion (LLIF) into one of two groups: direct decompression and indirect decompression.
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Oswestry Disability Index (ODI)
Timeframe: Up to 12 months post-operatively
Comparison of Oswestry Disability Index (ODI)
Timeframe: Up to 24 months post-operatively. (6 weeks, 3, 6, 12, and 24 months timepoints)