Clinical Trials Directory

Trials / Suspended

SuspendedNCT03726190

Clinical and Radiological Outcomes of Oblique Lateral Lumbar Interbody Fusion

Status
Suspended
Phase
Study type
Observational
Enrollment
303 (actual)
Sponsor
Tristate Brain and Spine Institute · Academic / Other
Sex
All
Age
Healthy volunteers
Not accepted

Summary

This study is undertaken to evaluate the outcomes of Oblique Lateral Lumbar Interbody Fusion (OLLIF). Specifically, the study seeks to measure outcomes on radiological imaging, outcomes reported by the patients on standardized questionnaires, and complication rates.

Conditions

Interventions

TypeNameDescription
PROCEDUREOblique Lateral Lumbar FusionOblique lateral lumbar interbody fusion (OLLIF) is a lumbar spinal fusion. OLLIF is performed with the patient in the prone position and employs an oblique lateral approach that enables the instrumentation to pass through Kambin's triangle which is defined as the space between the exiting nerve, the superior border of the caudal vertebra, and the superior articulating process of the inferior facet. This approach may be performed without direct visualization, guided by electrophysiological monitoring and biplanar fluoroscopy. During the approach, a blunt probe is used to make contact with the disc, followed by a series of gentle dilations. Discectomy is performed through a 10-mm access portal. The cage is inserted under continued electrophysiological monitoring and fluoroscopy.

Timeline

Start date
2013-01-01
Primary completion
2016-07-31
Completion
2025-12-31
First posted
2018-10-31
Last updated
2021-03-15

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT03726190. Inclusion in this directory is not an endorsement.

Clinical and Radiological Outcomes of Oblique Lateral Lumbar Interbody Fusion (NCT03726190) · Clinical Trials Directory