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A Clinical Study to Evaluate Safety and Performance of PEEK-OPTIMA™ HA Enhanced. | Clinical Trials | Clareo Health

COMPLETEDNANCT04416321

A Clinical Study to Evaluate Safety and Performance of PEEK-OPTIMA™ HA Enhanced.

The purpose of this trial is to collect clinical outcomes including radiographic and CT outcomes in patients who undergo spinal fusion using the Keos Lumbar Interbody Fusion Device.

Lead sponsor: Invibio Ltd•1 U.S. locations•View source on ClinicalTrials.gov

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Data from ClinicalTrials.govLast updated on ClinicalTrials.gov: January 29, 2026Terms

Trial snapshot

StatusCOMPLETED

PhaseNA

Enrollment25

Start dateJul 2021

Last updatedJan 29, 2026

Condition

Degenerative Disc Disease Spondylolisthesis Retrolisthesis

Locations shown

Neurosurgical Associates of Lancaster

Lancaster, Pennsylvania

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Data Source & Attribution

This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

ClinicalTrials.gov last update: January 29, 2026Data synced to Clareo: May 25, 2026

Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.

Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.

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A Clinical Study to Evaluate Safety and Performance of PEEK-OPTIMA™ HA Enhanced.

What this study is about

Save this trial guide to your notes

Sponsors

Related studies

Comparison of Clinical Outcomes, Complications Rate and Treatment Costs of Mini-TLIF and MIDLIF in the Treatment of Discogenic Low Back Pain

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Trial snapshot

Condition

Locations shown

For caregivers