Spine fusion study halted early: only 6 patients enrolled
NCT ID NCT05614284
First seen Dec 29, 2025 · Last updated Apr 29, 2026 · Updated 21 times
Summary
This study aimed to compare two bone graft materials (Virtuos and autograft) used during lumbar fusion surgery for patients with degenerative disc disease. The goal was to see which material led to better bone fusion rates at 12 and 24 months after surgery. However, the study was terminated early and only enrolled 6 participants, so no reliable conclusions can be drawn.
Disclaimer
Read more
Show less
This is a summary of
the original study
.
Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for DEGENERATIVE DISC DISEASE are added.
By submitting, you agree to our Terms of use
Contacts and locations
Show contact details
Enter your email to view the contact information for this study.
By submitting, you agree to our Terms of use
Locations
-
Central CT Neurosurgery & Spine
New Britain, Connecticut, 06051, United States
-
Michigan Brain and Spine
Royal Oak, Michigan, 48073, United States
-
University of Texas South Western
Dallas, Texas, 75390, United States
Conditions
Explore the condition pages connected to this study.