A Prospective Analysis of the Efficacy of Allosync Expand and Autograft Bone Graft in Open Lumbar Spinal Fusion

Spondylolisthesis, Grade 1 Clinical Trial

Official title:
A Prospective Analysis of the Efficacy of Allosync Expand and Autograft Bone Graft in Open Lumbar Spinal Fusion

Status Enrolling by invitation

Clinical Trial Summary

The purpose of this study is to assess the radiographic and clinical outcomes of spinal fusion following use of Allosync Expand and autograft bone graft.

Clinical Trial Description

This is a single site, prospective study with patients selected as study subjects from the Investigator's standard patient population who fulfill the Inclusion/Exclusion Criteria and agree to participate in the study. The study surgery is standard of care, with patients identified as requiring surgery prior to enrollment. The study surgery is lumbar posterior fixation with supplemental posterolateral fusion at from 1 to 3 levels. One side of the posterolateral fusion will be Allosync Expand (utilizing the BMA Angel kit to hydrate) and the other side to autograft bone (control). ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT06415110
Study type	Observational
Source	Research Source
Contact
Status	Enrolling by invitation
Phase
Start date	May 2024
Completion date	May 2027

View Details

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