Performance of Inductigraft in Spinal Fusion — APOLLO  

Degenerative Disk Disease Clinical Trial

Official title: A Prospective Open-label Non-randomdised Multi-centre Clinical Study to Evaluate the Performance of Inductigraft in Posterolateral Fusion

Status Completed

Clinical Trial Summary

This is an open-label non-randomised, prospective, post market study to evaluate the performance of Inductigraft (osteoinductive synthetic bone graft) in patients receiving posterolateral lumbar spine fusion through assessment of successful fusion at 12 months post operation using x-rays and CT scans. Quality of life questionnaires also used to assess clinical outcome measures such as pain and quality of life. Patients followed up for 24 months after surgery.

Clinical Trial Description

n/a

Related Conditions & MeSH terms

• Degenerative Disk Disease
• Intervertebral Disc Degeneration
• Spinal Stenosis
• Spinal Stenosis of Lumbar Region

• NCT number: NCT01452022
• Study type: Interventional
• Source: Baxter Healthcare Corporation
• Status: Completed
• Phase: N/A
• Start date: October 2011
• Completion date: August 2015