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Clinical Trial Summary

The primary objective of this study is to measure the success rate of lumbar fusion in subjects at 12 months when instrumented lumbar arthrodesis is performed using OssiMend Bioactive Moldable as the bone grafting material


Clinical Trial Description

The primary objective of this study is to measure the success rate of lumbar fusion in subjects at 12 months when instrumented lumbar arthrodesis is performed using OssiMend Bioactive Moldable as the bone grafting material. The primary endpoints are radiographic evidence of fusion and the absence of serious adverse events attributable to OssiMend Bioactive Moldable. The secondary objective is to evaluate the clinical outcomes over a period of 1 year (2 years, if possible). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04775537
Study type Observational
Source Collagen Matrix
Contact Mohamed Moawad
Phone 2014051477
Email mmoawad@collagenmatrix.com
Status Recruiting
Phase
Start date January 21, 2021
Completion date August 21, 2023

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