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Clinical Trial Summary

Currently there is no consensus on the best surgical treatment of patients with symptomatic isthmic spondylolisthesis (IS). Clinical equipoise exists amongst experienced clinicians on the various surgical techniques available. This study will involve multiple phases to answer specific research questions comparing anterior and posterior interbody fusion in patients with lumbar isthmic spondylolisthesis. The primary end point will be 1-year proportions of patients reaching minimal clinically important difference (MCID) in terms of leg pain measured by NRS leg. The secondary endpoints will be predetermined moderate to severe AEs, reoperations for nonunion, symptomatic adjacent segment disease, radiological alignment correction and correlation with HRQOL as well as economic analysis at 1, 2, 5 and 10 years.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05701046
Study type Observational
Source University of British Columbia
Contact Charlotte Dandurand
Phone (604) 875-5859
Email charlotte.dandurand@vch.ca
Status Recruiting
Phase
Start date January 5, 2023
Completion date February 15, 2038

See also
  Status Clinical Trial Phase
Not yet recruiting NCT04559399 - Smiley Face Shaped Rod Technique Versus Instrumented Posteriolateral Fusion in Treatment of Isthmic Lumbar Spondylolisthesis N/A
Completed NCT02564705 - Comparative Study of Anterior vs. Posterior Surgical Treatment for Lumbar Isthmic Spondylolisthesis
Completed NCT04968626 - Relationship Between Spinopelvic Parameters and Clinical Symptoms of Low-grade Lumbar Isthmic Spondylolisthesis N/A
Completed NCT03585439 - Isthmic Spondylolisthesis Treated With Combined Approach: Clinical and Radiological Outcomes
Terminated NCT03507881 - Prospective Study on Ennovate® Pedicle Screw Fixation in Isthmic Spondylolisthesis Patients
Withdrawn NCT03640338 - The Efficacy of Continuous Cold-Therapy on Postoperative Pain and Narcotics Use Following Spinal Fusion N/A