Trials / Active Not Recruiting
Active Not RecruitingNCT06876311
Observational Study to Evaluate the STALIF® C FLX, STALIF® M FLX, STALIF® L FLX Cages and FORTOS-C®
Sponsor-initiated, Retrospective, Monocentric, Non-interventional Clinical Observational Study to Evaluate the STALIF® C FLX, STALIF® M FLX, STALIF® L FLX Cages and FORTOS-C®
- Status
- Active Not Recruiting
- Phase
- —
- Study type
- Observational
- Enrollment
- 100 (estimated)
- Sponsor
- Silony Medical GmbH · Industry
- Sex
- All
- Age
- 21 Years
- Healthy volunteers
- Not accepted
Summary
Post-operative clinical outcome data on the devices used to treat spinal diseases are collected and evaluated in order to analyze the safety and performance of the implants used.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Anterior Cervical Interbody Fusion | Standard Anterior Cervical Interbody Fusion with Stand-alone Cervical Cages |
| DEVICE | Anterior lumbar Interbody Fusion | Standard Anterior Lumbar Interbody Fusion with Stand-Alone Lumbar Cages |
| DEVICE | Lateral Lumbar Interbody Fusion | Standard Lateral Lumbar Interbody Fusion with Stand-alone Lumbar cage |
Timeline
- Start date
- 2025-03-04
- Primary completion
- 2025-04-30
- Completion
- 2025-05-30
- First posted
- 2025-03-14
- Last updated
- 2025-03-14
Locations
1 site across 1 country: United States
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT06876311. Inclusion in this directory is not an endorsement.