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More info
You can access this
clinical trial
if you have
Degenerative Disk Disease or Spinal Stenosis of Lumbar Region
and you are
over 18
years old
-
The phase for this study is not defined.
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The purpose

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.

Provided treatments

  • Device: Inductigraft

Locations near you

Unfortunately, there are no recruiting locations near you. Please check the list with all locations below.
Tris trial is registered with FDA with number: NCT01452022. The sponsor of the trial is Baxter Healthcare Corporation and it is looking for 125 volunteers for the current phase.
Official trial title:
A Prospective Open-label Non-randomdised Multi-centre Clinical Study to Evaluate the Performance of Inductigraft in Posterolateral Fusion