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The Clinical Study to Evaluate the Efficacy and Safety of Novosis in Posterolateral Fusion
The purpose of this study is to evaluate the efficacy and safety of Novosis in posterolateral fusion
Details
| Lead sponsor | BioAlpha Inc. |
|---|---|
| Phase | NA |
| Status | UNKNOWN |
| Enrolment | 90 |
| Start date | 2013-03 |
| Completion | 2016-03 |
Conditions
- Posterolateral Fusion
Interventions
- Novosis
- Iliac crest bone graft
Primary outcomes
- Fusion grade by CT assessments after surgery — 24 weeks
Countries
South Korea