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Grade 1 Spondylolisthesis clinical trials

View clinical trials related to Grade 1 Spondylolisthesis.

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NCT ID: NCT05610397 Not yet recruiting - Clinical trials for Degenerative Disc Disease

Retrospective Study With Patients Treated With STALIF® C or M and Ti or FLX Implants for 1 and 2 Levels

Stalif
Start date: April 24, 2023
Phase:
Study type: Observational

This is a Retrospective, Observational Multi-Center study, utilizing patients diagnosed with up to a Grade1 spondylolisthesis or retrolisthesis or symptomatic degenerative disc disease and treated with STALIF® C, or M, Ti and/or FLX implants at one or two levels.

NCT ID: NCT04584619 Active, not recruiting - Clinical trials for Degenerative Disc Disease

Idys™ TLIF 3DTi Post Market Clinical Follow-up

Start date: October 1, 2020
Phase:
Study type: Observational

The aim of this observational post-marketing study is to provide additional information on the safety and effectiveness of Idys™ TLIF 3DTi at up to 24 months post transforaminal lumbar fusion in usual surgical practice.

NCT ID: NCT03570801 Terminated - Clinical trials for Lumbar Spinal Stenosis

SLIP II Registry: Spinal Laminectomy Versus Instrumented Pedicle Screw Fusion

SLIPII
Start date: October 17, 2017
Phase: N/A
Study type: Interventional

The purpose of the project is to perform an RCT comparing patient satisfaction and outcome with or without the use of an expert panel. The purpose is also to create a registry to compare the effectiveness of decompression alone versus decompression with fusion for patients with degenerative grade I spondylolisthesis and symptomatic lumbar spinal stenosis. Primary analysis will focus on the patients' improvement from baseline patient-reported outcome questionnaires. In addition, the SLIP II registry aims to (i) develop an algorithm which could identify cases in which surgical experts are likely to recommend one treatment (i.e. >80% of experts recommend one form of treatment) and (ii) develop a radiology-based machine learning algorithm that would prospectively classify patients as either 'stable' or 'unstable.' In addition to patient reported outcomes, step counts will be collected in order to determine the correlation of step count with patient-reported outcomes (ODI and EQ-5D) and the need for re-operation. This registry portion of the study aims to prospectively collect comparative data for these patients treated with either decompression alone or decompression with fusion.

NCT ID: NCT02068729 Terminated - Clinical trials for Degenerative Disc Disease

Comparison of Complication Rates Between Lateral Approaches to the Lumbar Spine

RAVINE
Start date: June 2014
Phase:
Study type: Observational

An evaluation of the incidence of complications resulting from far lateral spine surgery utilizing the K2M RAVINE® Lateral Access System (RAVINE) with ALEUTIAN® Lateral Interbody Spacer System versus literature reported results for the NuVasive XLIF® system (XLIF) in the treatment of degenerative disc disease (DDD) with up to Grade 1 spondylolisthesis.