Multi-Center Prospective Study Evaluation Aspen Spinous Process Fixation System for Use in Posterolateral Fusion (PLF) in Patients With Spondylolisthesis
This study has suspended participant recruitment.
Sponsor:
Lanx, Inc.
Information provided by (Responsible Party):
Lanx, Inc.
ClinicalTrials.gov Identifier:
NCT01560273
First received: March 15, 2012
Last updated: May 3, 2013
Last verified: May 2012
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No Study Results Posted on ClinicalTrials.gov for this Study
| Study Status: | This study has suspended participant recruitment. |
|---|---|
| Estimated Study Completion Date: | May 2015 |
| Estimated Primary Completion Date: | May 2014 (Final data collection date for primary outcome measure) |