CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 29 enrolled
Drug / intervention
Posterolateral Fusionprocedure
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT01873586
NCT01873586N/ACompleted
CompareCT.gov

Efficacy and Safety of OsteoStrux™ Collagen Ceramic Scaffold in Instrumented Lumbar Spine Fusion

SeaSpine, Inc.·interventional·Posted Jun 10, 2013·Updated Jun 17, 2019

In Brief

A clinical study evaluating Posterolateral Fusion for Degenerative Changes and 2 related conditions. Completed, enrolled 29 participants across 1 site.

Detailed Summary

The objective of this study is to prospectively evaluate the performance of Integra's OsteoStrux Collagen Ceramic Scaffold combined with bone marrow aspirate as an adjunct for instrumented posterolateral spine fusion, as compared to local autograft.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsDegenerative Changes, Stenosis, Spondylosis
CountriesUnited States
Collaborators--

Timeline

N/ACompletedFinished
20132014201520162017201820192020202120222023202420252026
First PostedJun 10, 2013
Enrollment StartOct 1, 2012
Primary CompletionOct 1, 2016
TodayJul 2, 2026
Enrollment to primary: 4 yearsPosted 13.1 years ago

Interventions

Posterolateral Fusionprocedure