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MLX/XLX ACR Expandable Lumbar Interbody Implants

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Contents

clinicaltrials.gov/study/NCT04420143
Is a
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Clinical study
0

Clinical Study attributes

NCT Number
NCT044201430
Health Conditions in Trial
Spondylolisthesis
Spondylolisthesis
0
‌
Degenerative Scoliosis
0
Degenerative disc disease
Degenerative disc disease
0
Trial Recruitment Size
1090
Trial Sponsor
NuVasive
NuVasive
0
Clinical Trial Start Date
January 27, 2020
0
Primary Completion Date
October 23, 2020
0
Study Completion Date
October 23, 2020
0
Clinical Trial Study Type
Observational0
Observational Clinical Trial Type
Cohort0
Observational Study Perspective
Retrospective0
Participating Facility
‌
orthopaedic specialty Institute
0
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Carolina Neurosurgery & Spine Associates
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Official Name
An Assessment of the Safety and Performance of the MLX® Medial Lateral and XLX ACR® Expandable Lumbar Interbody Implants for the Treatment of Patients With Degenerative Conditions of the Thoracic and/or Lumbar Spine0
Last Updated
August 24, 2021
0
Study summary

The objective of this study is to evaluate the safety and performance of thoracic and/or lumbar spine surgery using the MLX and XLX ACR interbody implants as measured by reported complications, radiographic outcomes, and clinical patient outcomes. This study is being undertaken to identify possible residual risks and to clarify mid- to long-term clinical performance that may affect the benefit/risk ratios of the MLX and XLX ACR interbody implants.

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