CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 178 enrolled
Drug / intervention
Interbody Fusiondevice
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/NCT01323387
NCT01323387N/ACompleted

Lumbar Degenerative Disc Disease Treated With

Synthes USA HQ, Inc.·interventional·Posted Mar 25, 2011·Updated Jan 16, 2018

In Brief

A clinical study evaluating Interbody Fusion for Lumbar Degenerative Disc Disease. Completed, enrolled 178 participants.

Detailed Summary

Multi-center, prospective nonrandomized study of treatment for 1 and 2 level degenerative disc disease between L2 and S1. Patients will be followed for a minimum of 2 years. The primary objective of this study to measure fusion success in patients with lumbar degenerative disc disease using the ATB and ALIF/FRA Spacer. The Secondary objective is evaluation of the patient's quality of life, pain and function.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
Countries--
Collaborators--

Timeline

N/ACompletedFinished
200420052006200720082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedMar 25, 2011
Enrollment StartApr 1, 2004
Primary CompletionMay 1, 2009
Study CompletionFeb 1, 2011
TodayJul 2, 2026
Enrollment to primary: 5.1 yearsPosted 15.3 years ago

Interventions

Interbody Fusiondevice

allograft spacer + anterior plate